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Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management (CORTICAU)

Primary Purpose

Caustic Esophageal Injury, Esophageal Stenosis, Pharyngeal Stenosis

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Methylprednisolone
Placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Caustic Esophageal Injury focused on measuring Caustic, Esophageal Stenosis, Pharyngeal Stenosis, Corticosteroid treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  • Age greater than or equal to 18 years
  • Recent caustic product ingestion (time between taking the product and initiating the evaluated treatment or placebo between 6 and 24 hours after ingestion)
  • Predictive CT criteria for high-risk esophageal stenosis (grade IIb) in its most pathological part
  • Written, signed consent (trusted person if necessary, in case of impossibility of collection)
  • Beneficiary of a social security system

Exclusion Criteria:

  • Indication of resection or surgical exploration in emergency
  • History of caustic ingestion
  • Corticosteroids taken at a dose greater than 20 mg prednisone within 7 days before randomization
  • Contraindication to corticosteroid therapy:
  • Any infectious condition that required antibiotic treatment within 7 days of randomization
  • Any vaccine living within 7 days of randomization
  • Hypersensitivity to one of the components
  • Pregnancy in progress
  • Breastfeeding in progress
  • Co-intoxication involving vital prognosis and requiring, according to the patient's doctor, intensive care management
  • Patient under guardianship or curatorship

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Methylprednisolone

    Placebo (no corticosteroid treatment)

    Arm Description

    Dose: 500mg/day for the first two days then 2mg/kg per day for three days. Dilution in 0.9% NaCl, 100 ml as a single slow intravenous administration over 60 minutes Total processing time of 5 days

    NaCl 0.9%, 100ml per day as a single slow intravenous administration over 60 minutes for a total treatment duration of 5 days

    Outcomes

    Primary Outcome Measures

    Indication for esophageal or pharyngeal surgical reconstruction
    The primary outcome is the indication for esophageal or pharyngeal surgical reconstruction due to: The occurrence of one or more esophageal stenosis refractory to endoscopic dilation within 12 months of ingestion, as defined by: The need for more than 5 sessions of esophageal endoscopic dilation Non-expandable stenosis or esophageal obstruction; An esophageal perforation that occurs during dilation, which contraindicates the continuation of dilation. The occurrence of pharyngeal stenosis, defined by the need to perform pharyngoplasty.

    Secondary Outcome Measures

    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Delay in the occurrence of refractory esophagal stenosis or pharyngeal stenosis
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Distance of the stenosis
    Distance between the stenosis and the dental arches (cm)
    Distance of the stenosis
    Distance between the stenosis and the dental arches (cm)
    Distance of the stenosis
    Distance between the stenosis and the dental arches (cm)
    Distance of the stenosis
    Distance between the stenosis and the dental arches (cm)
    Distance of the stenosis
    Distance between the stenosis and the dental arches (cm)
    Number of stenosis
    Number of stenosis will be evaluated by endoscopy
    Number of stenosis
    Number of stenosis will be evaluated by endoscopy
    Number of stenosis
    Number of stenosis will be evaluated by endoscopy
    Number of stenosis
    Number of stenosis will be evaluated by endoscopy
    Number of stenosis
    Number of stenosis will be evaluated by endoscopy
    Length of stenosis
    Length of each stenosis will be evaluated by endoscopy
    Length of stenosis
    Length of each stenosis will be evaluated by endoscopy
    Length of stenosis
    Length of each stenosis will be evaluated by endoscopy
    Length of stenosis
    Length of each stenosis will be evaluated by endoscopy
    Length of stenosis
    Length of each stenosis will be evaluated by endoscopy
    Estimated diameter of stenosis
    Diameter of each stenosis will be evaluated by endoscopy
    Estimated diameter of stenosis
    Diameter of each stenosis will be evaluated by endoscopy
    Estimated diameter of stenosis
    Diameter of each stenosis will be evaluated by endoscopy
    Estimated diameter of stenosis
    Diameter of each stenosis will be evaluated by endoscopy
    Estimated diameter of stenosis
    Diameter of each stenosis will be evaluated by endoscopy
    Endoluminal inflammation
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Endoluminal inflammation
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Endoluminal inflammation
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Endoluminal inflammation
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Endoluminal inflammation
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Number of dilation sessions
    Number of dilation sessions evaluated by endoscopy
    Number of dilation sessions
    Number of dilation sessions evaluated by endoscopy
    Number of dilation sessions
    Number of dilation sessions evaluated by endoscopy
    Number of dilation sessions
    Number of dilation sessions evaluated by endoscopy
    Number of dilation sessions
    Number of dilation sessions evaluated by endoscopy
    Intervals between iterative dilations
    Time between endoscopic dilatations if necessary iterative dilation
    Intervals between iterative dilations
    Time between endoscopic dilatations if necessary iterative dilation
    Intervals between iterative dilations
    Time between endoscopic dilatations if necessary iterative dilation
    Intervals between iterative dilations
    Time between endoscopic dilatations if necessary iterative dilation
    Intervals between iterative dilations
    Time between endoscopic dilatations if necessary iterative dilation
    Digestive perforations
    Proportion of digestive perforations secondary to endoscopic dilation
    Digestive perforations
    Proportion of digestive perforations secondary to endoscopic dilation
    Digestive perforations
    Proportion of digestive perforations secondary to endoscopic dilation
    Digestive perforations
    Proportion of digestive perforations secondary to endoscopic dilation
    Digestive perforations
    Proportion of digestive perforations secondary to endoscopic dilation
    Extent of pharyngeal stenosis
    Laryngeal stenosis associated with pharyngeal stenosis
    Extent of pharyngeal stenosis
    Laryngeal stenosis associated with pharyngeal stenosis
    Extent of pharyngeal stenosis
    Laryngeal stenosis associated with pharyngeal stenosis
    Extent of pharyngeal stenosis
    Laryngeal stenosis associated with pharyngeal stenosis
    Extent of pharyngeal stenosis
    Laryngeal stenosis associated with pharyngeal stenosis
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of unanticipated adverse reactions
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Proportion of adverse reactions related to corticosteroid therapy
    Adverse reactions related to corticosteroid therapy will be defined by the occurrence of infections needing antibiotic therapy or spontaneous digestive perforation or digestive bleeding or cardiac arrhythmias de novo or pulmonary edema requiring treatment (increased oxygen requirements and/or Diuretic and/or Vasodilator and/or non-invasive ventilation and/or invasive ventilation) or respiratory complications (High blood pressure requiring treatment - Metabolic alkalosis- Hypokalemia<3.0mmol/l - Delirium- Decompensation of a psychiatric pathology)
    C-Reactive Protein (CRP)
    Inflammation markers
    C-Reactive Protein (CRP)
    Inflammation markers
    C-Reactive Protein (CRP)
    Inflammation markers
    C-Reactive Protein (CRP)
    Inflammation markers
    interleukin-1 (IL1)
    Inflammation markers
    interleukin-1 (IL1)
    Inflammation markers
    interleukin-1 (IL1)
    Inflammation markers
    interleukin-1 (IL1)
    Inflammation markers
    interleukin-6 (IL-6)
    Inflammation markers
    interleukin-6 (IL-6)
    Inflammation markers
    interleukin-6 (IL-6)
    Inflammation markers
    interleukin-6 (IL-6)
    Inflammation markers
    Tumour Necrosis Factor alpha (TNF alpha)
    Inflammation markers
    Tumour Necrosis Factor alpha (TNF alpha)
    Inflammation markers
    Tumour Necrosis Factor alpha (TNF alpha)
    Inflammation markers
    Tumour Necrosis Factor alpha (TNF alpha)
    Inflammation markers
    Tissue Growth Factor Beta (TGF beta)
    Fibrosis markers
    Tissue Growth Factor Beta (TGF beta)
    Fibrosis markers
    Tissue Growth Factor Beta (TGF beta)
    Fibrosis markers
    Tissue Growth Factor Beta (TGF beta)
    Fibrosis markers
    Galectin 3
    Fibrosis markers
    Galectin 3
    Fibrosis markers
    Galectin 3
    Fibrosis markers
    Galectin 3
    Fibrosis markers

    Full Information

    First Posted
    November 28, 2018
    Last Updated
    November 28, 2018
    Sponsor
    Assistance Publique - Hôpitaux de Paris
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03760354
    Brief Title
    Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management
    Acronym
    CORTICAU
    Official Title
    Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management for the Prevention of Refractory Stenosis of the Esophagus and Pharynx- The CORTICAU Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 15, 2019 (Anticipated)
    Primary Completion Date
    February 15, 2020 (Anticipated)
    Study Completion Date
    February 15, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique - Hôpitaux de Paris

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The management of patients who have ingested a caustic product has changed since 2007. Whereas previously the lesion assessment and surgical indication were based on endoscopic data, the therapeutic algorithm is currently based solely on the results of a CT scan with contrast injection, performed 6 hours after ingestion. This examination makes it possible to reliably assess the viability of the esophageal and gastric walls and thus to indicate digestive resection. The therapeutic consequences of this new treatment are important because, by expanding the indications for conservative treatment after severe ingestion, it brings a significant gain in terms of survival, morbidity and functional outcome. In the absence of emergency digestive resection, however, the functional prognosis is often overshadowed by the formation of esophageal stenosis in the months following ingestion. Patients then require endoscopic dilation treatment. In the event of failure or impossibility of dilation, which defines refractory stenosis, esophageal reconstruction is necessary. In case of sequential pharyngeal stenosis following ingestion, esophageal and pharyngeal reconstruction is indicated as a first-line treatment, since these stenosis do not respond to endoscopic dilations. The expansion of the indications for conservative treatment after severe ingestion using CT scans has led to an increase in the incidence of after-effect stenosis. We aim to develop a therapeutic approach that will prevent the development of refractory and pharyngeal esophageal stenosis. Indeed, there is currently no strategy that has proven effective in this regard in adults. The value of corticosteroid therapy for the prevention of caustic stenosis has only been evaluated in children and remains controversial. The main objective is to evaluate the effect of early systemic corticosteroid therapy on the risk of refractory esophageal or pharyngeal stenosis within one year of ingestion of a caustic substance in a population of patients at high risk of stenosis, defined according to tomodensitometric criteria (grade IIb: severe lesions, absence of transparietal necrosis), and for whom there is no indication of urgent digestive resection.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Caustic Esophageal Injury, Esophageal Stenosis, Pharyngeal Stenosis
    Keywords
    Caustic, Esophageal Stenosis, Pharyngeal Stenosis, Corticosteroid treatment

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Model Description
    Prospective Phase II, Bayesian, single-blinded, monocentric, randomized, prospective clinical trial
    Masking
    Participant
    Masking Description
    single-blinded trial
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Methylprednisolone
    Arm Type
    Experimental
    Arm Description
    Dose: 500mg/day for the first two days then 2mg/kg per day for three days. Dilution in 0.9% NaCl, 100 ml as a single slow intravenous administration over 60 minutes Total processing time of 5 days
    Arm Title
    Placebo (no corticosteroid treatment)
    Arm Type
    Placebo Comparator
    Arm Description
    NaCl 0.9%, 100ml per day as a single slow intravenous administration over 60 minutes for a total treatment duration of 5 days
    Intervention Type
    Drug
    Intervention Name(s)
    Methylprednisolone
    Other Intervention Name(s)
    Corticosteroid treatment
    Intervention Description
    Dose: 500mg/day for the first two days then 2mg/kg per day for three days. Dilution in 0.9% NaCl, 100 ml as a single slow intravenous administration over 60 minutes Total processing time of 5 days
    Intervention Type
    Other
    Intervention Name(s)
    Placebo
    Other Intervention Name(s)
    Control Arm
    Intervention Description
    NaCl 0.9%, 100ml per day as a single slow intravenous administration over 60 minutes for a total treatment duration of 5 days
    Primary Outcome Measure Information:
    Title
    Indication for esophageal or pharyngeal surgical reconstruction
    Description
    The primary outcome is the indication for esophageal or pharyngeal surgical reconstruction due to: The occurrence of one or more esophageal stenosis refractory to endoscopic dilation within 12 months of ingestion, as defined by: The need for more than 5 sessions of esophageal endoscopic dilation Non-expandable stenosis or esophageal obstruction; An esophageal perforation that occurs during dilation, which contraindicates the continuation of dilation. The occurrence of pharyngeal stenosis, defined by the need to perform pharyngoplasty.
    Time Frame
    within 12 months post ingestion
    Secondary Outcome Measure Information:
    Title
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Description
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Time Frame
    at 1 month
    Title
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Description
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Time Frame
    at 3 months
    Title
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Description
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Time Frame
    at 6 months
    Title
    Delay in the occurrence of refractory stenosis or pharyngeal stenosis
    Description
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Time Frame
    at 9 months
    Title
    Delay in the occurrence of refractory esophagal stenosis or pharyngeal stenosis
    Description
    Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
    Time Frame
    at 12 months
    Title
    Distance of the stenosis
    Description
    Distance between the stenosis and the dental arches (cm)
    Time Frame
    at 1 month
    Title
    Distance of the stenosis
    Description
    Distance between the stenosis and the dental arches (cm)
    Time Frame
    at 3 months
    Title
    Distance of the stenosis
    Description
    Distance between the stenosis and the dental arches (cm)
    Time Frame
    at 6 months
    Title
    Distance of the stenosis
    Description
    Distance between the stenosis and the dental arches (cm)
    Time Frame
    at 9 months
    Title
    Distance of the stenosis
    Description
    Distance between the stenosis and the dental arches (cm)
    Time Frame
    at 12 months
    Title
    Number of stenosis
    Description
    Number of stenosis will be evaluated by endoscopy
    Time Frame
    at 1 month
    Title
    Number of stenosis
    Description
    Number of stenosis will be evaluated by endoscopy
    Time Frame
    at 3 months
    Title
    Number of stenosis
    Description
    Number of stenosis will be evaluated by endoscopy
    Time Frame
    at 6 months
    Title
    Number of stenosis
    Description
    Number of stenosis will be evaluated by endoscopy
    Time Frame
    at 9 months
    Title
    Number of stenosis
    Description
    Number of stenosis will be evaluated by endoscopy
    Time Frame
    at 12 months
    Title
    Length of stenosis
    Description
    Length of each stenosis will be evaluated by endoscopy
    Time Frame
    at 1 month
    Title
    Length of stenosis
    Description
    Length of each stenosis will be evaluated by endoscopy
    Time Frame
    at 3 months
    Title
    Length of stenosis
    Description
    Length of each stenosis will be evaluated by endoscopy
    Time Frame
    at 6 months
    Title
    Length of stenosis
    Description
    Length of each stenosis will be evaluated by endoscopy
    Time Frame
    at 9 months
    Title
    Length of stenosis
    Description
    Length of each stenosis will be evaluated by endoscopy
    Time Frame
    at 12 months
    Title
    Estimated diameter of stenosis
    Description
    Diameter of each stenosis will be evaluated by endoscopy
    Time Frame
    at 1 month
    Title
    Estimated diameter of stenosis
    Description
    Diameter of each stenosis will be evaluated by endoscopy
    Time Frame
    at 3 months
    Title
    Estimated diameter of stenosis
    Description
    Diameter of each stenosis will be evaluated by endoscopy
    Time Frame
    at 6 months
    Title
    Estimated diameter of stenosis
    Description
    Diameter of each stenosis will be evaluated by endoscopy
    Time Frame
    at 9 months
    Title
    Estimated diameter of stenosis
    Description
    Diameter of each stenosis will be evaluated by endoscopy
    Time Frame
    at 12 months
    Title
    Endoluminal inflammation
    Description
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Time Frame
    at 1 month
    Title
    Endoluminal inflammation
    Description
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Time Frame
    at 3 months
    Title
    Endoluminal inflammation
    Description
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Time Frame
    at 6 months
    Title
    Endoluminal inflammation
    Description
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Time Frame
    at 9 months
    Title
    Endoluminal inflammation
    Description
    Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
    Time Frame
    at 12 months
    Title
    Number of dilation sessions
    Description
    Number of dilation sessions evaluated by endoscopy
    Time Frame
    at 1 month
    Title
    Number of dilation sessions
    Description
    Number of dilation sessions evaluated by endoscopy
    Time Frame
    at 3 months
    Title
    Number of dilation sessions
    Description
    Number of dilation sessions evaluated by endoscopy
    Time Frame
    at 6 months
    Title
    Number of dilation sessions
    Description
    Number of dilation sessions evaluated by endoscopy
    Time Frame
    at 9 months
    Title
    Number of dilation sessions
    Description
    Number of dilation sessions evaluated by endoscopy
    Time Frame
    at 12 months
    Title
    Intervals between iterative dilations
    Description
    Time between endoscopic dilatations if necessary iterative dilation
    Time Frame
    at 1 month
    Title
    Intervals between iterative dilations
    Description
    Time between endoscopic dilatations if necessary iterative dilation
    Time Frame
    at 3 months
    Title
    Intervals between iterative dilations
    Description
    Time between endoscopic dilatations if necessary iterative dilation
    Time Frame
    at 6 months
    Title
    Intervals between iterative dilations
    Description
    Time between endoscopic dilatations if necessary iterative dilation
    Time Frame
    at 9 months
    Title
    Intervals between iterative dilations
    Description
    Time between endoscopic dilatations if necessary iterative dilation
    Time Frame
    at 12 months
    Title
    Digestive perforations
    Description
    Proportion of digestive perforations secondary to endoscopic dilation
    Time Frame
    at 1 month
    Title
    Digestive perforations
    Description
    Proportion of digestive perforations secondary to endoscopic dilation
    Time Frame
    at 3 months
    Title
    Digestive perforations
    Description
    Proportion of digestive perforations secondary to endoscopic dilation
    Time Frame
    at 6 months
    Title
    Digestive perforations
    Description
    Proportion of digestive perforations secondary to endoscopic dilation
    Time Frame
    at 9 months
    Title
    Digestive perforations
    Description
    Proportion of digestive perforations secondary to endoscopic dilation
    Time Frame
    at 12 months
    Title
    Extent of pharyngeal stenosis
    Description
    Laryngeal stenosis associated with pharyngeal stenosis
    Time Frame
    at 1 month
    Title
    Extent of pharyngeal stenosis
    Description
    Laryngeal stenosis associated with pharyngeal stenosis
    Time Frame
    at 3 months
    Title
    Extent of pharyngeal stenosis
    Description
    Laryngeal stenosis associated with pharyngeal stenosis
    Time Frame
    at 6 months
    Title
    Extent of pharyngeal stenosis
    Description
    Laryngeal stenosis associated with pharyngeal stenosis
    Time Frame
    at 9 months
    Title
    Extent of pharyngeal stenosis
    Description
    Laryngeal stenosis associated with pharyngeal stenosis
    Time Frame
    at 12 months
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at day 0
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at day 2
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at day 5
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at day 7
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at one month
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at 3 months
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at 6 months
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at 9 months
    Title
    Proportion of unanticipated adverse reactions
    Description
    Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay > 24 ICU
    Time Frame
    at 12 months
    Title
    Proportion of adverse reactions related to corticosteroid therapy
    Description
    Adverse reactions related to corticosteroid therapy will be defined by the occurrence of infections needing antibiotic therapy or spontaneous digestive perforation or digestive bleeding or cardiac arrhythmias de novo or pulmonary edema requiring treatment (increased oxygen requirements and/or Diuretic and/or Vasodilator and/or non-invasive ventilation and/or invasive ventilation) or respiratory complications (High blood pressure requiring treatment - Metabolic alkalosis- Hypokalemia<3.0mmol/l - Delirium- Decompensation of a psychiatric pathology)
    Time Frame
    within 7 days
    Title
    C-Reactive Protein (CRP)
    Description
    Inflammation markers
    Time Frame
    at day 0
    Title
    C-Reactive Protein (CRP)
    Description
    Inflammation markers
    Time Frame
    at day 2
    Title
    C-Reactive Protein (CRP)
    Description
    Inflammation markers
    Time Frame
    at day 5
    Title
    C-Reactive Protein (CRP)
    Description
    Inflammation markers
    Time Frame
    at one month
    Title
    interleukin-1 (IL1)
    Description
    Inflammation markers
    Time Frame
    at day 0
    Title
    interleukin-1 (IL1)
    Description
    Inflammation markers
    Time Frame
    at day 2
    Title
    interleukin-1 (IL1)
    Description
    Inflammation markers
    Time Frame
    at day 5
    Title
    interleukin-1 (IL1)
    Description
    Inflammation markers
    Time Frame
    at one month
    Title
    interleukin-6 (IL-6)
    Description
    Inflammation markers
    Time Frame
    at day 0
    Title
    interleukin-6 (IL-6)
    Description
    Inflammation markers
    Time Frame
    at day 2
    Title
    interleukin-6 (IL-6)
    Description
    Inflammation markers
    Time Frame
    at day 5
    Title
    interleukin-6 (IL-6)
    Description
    Inflammation markers
    Time Frame
    at one month
    Title
    Tumour Necrosis Factor alpha (TNF alpha)
    Description
    Inflammation markers
    Time Frame
    at day 0
    Title
    Tumour Necrosis Factor alpha (TNF alpha)
    Description
    Inflammation markers
    Time Frame
    at day 2
    Title
    Tumour Necrosis Factor alpha (TNF alpha)
    Description
    Inflammation markers
    Time Frame
    at day 5
    Title
    Tumour Necrosis Factor alpha (TNF alpha)
    Description
    Inflammation markers
    Time Frame
    at one month
    Title
    Tissue Growth Factor Beta (TGF beta)
    Description
    Fibrosis markers
    Time Frame
    at day 0
    Title
    Tissue Growth Factor Beta (TGF beta)
    Description
    Fibrosis markers
    Time Frame
    at day 2
    Title
    Tissue Growth Factor Beta (TGF beta)
    Description
    Fibrosis markers
    Time Frame
    at day 5
    Title
    Tissue Growth Factor Beta (TGF beta)
    Description
    Fibrosis markers
    Time Frame
    at one month
    Title
    Galectin 3
    Description
    Fibrosis markers
    Time Frame
    at day 0
    Title
    Galectin 3
    Description
    Fibrosis markers
    Time Frame
    at day 2
    Title
    Galectin 3
    Description
    Fibrosis markers
    Time Frame
    at day 5
    Title
    Galectin 3
    Description
    Fibrosis markers
    Time Frame
    at one month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria Age greater than or equal to 18 years Recent caustic product ingestion (time between taking the product and initiating the evaluated treatment or placebo between 6 and 24 hours after ingestion) Predictive CT criteria for high-risk esophageal stenosis (grade IIb) in its most pathological part Written, signed consent (trusted person if necessary, in case of impossibility of collection) Beneficiary of a social security system Exclusion Criteria: Indication of resection or surgical exploration in emergency History of caustic ingestion Corticosteroids taken at a dose greater than 20 mg prednisone within 7 days before randomization Contraindication to corticosteroid therapy: Any infectious condition that required antibiotic treatment within 7 days of randomization Any vaccine living within 7 days of randomization Hypersensitivity to one of the components Pregnancy in progress Breastfeeding in progress Co-intoxication involving vital prognosis and requiring, according to the patient's doctor, intensive care management Patient under guardianship or curatorship
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Helene CORTE
    Phone
    01.42.49.49.49
    Email
    helene.corte@aphp.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Marie-Quitterie PICAT
    Phone
    01.42.49.97.42
    Email
    marie-quitterie.picat@aphp.fr

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management

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