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
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
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
NCT ID
NCT03760354
First Posted
November 28, 2018
Last Updated
November 28, 2018
Sponsor
Assistance Publique - Hôpitaux de Paris
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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