search
Back to results

Dexamethasone, Can it Replace Ketoprofen in the Strategy of Intraoperative Multimodal Analgesia in Paediatric Surgery ? A Prospective Randomized Double-blinded Study. DEXA OP (DEXA OP)

Primary Purpose

Postoperative Nausea and Vomiting

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Dexamethasone 0.2 mg/kg
Dexamethasone 0.4 mg/kg
Ketoprofen 1 mg/kg
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Nausea and Vomiting focused on measuring Paediatric surgery

Eligibility Criteria

1 Year - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children, aged 1 to 16 years
  • Undergoing surgery (orchiopexy, inguinal hernia, circumcision, adenoidectomy, tonsillectomy or orthopedic act with osteosynthesis)
  • Parental consent

Exclusion Criteria:

  • Contraindication to NSAI or DXM
  • Hypersensitivity to ketoprofen, DXM, hypnovel or atarax
  • Porphyria
  • Long QT Syndrome
  • Renal or hepatic impairment
  • Corticosteroid consumption the week before surgery
  • NSAI consumption within 48 hours before surgery
  • IV induction for full stomach or myopathic patient.
  • French language not spoken by parents.
  • Simultaneous participation in biomedical research on health products

Sites / Locations

  • Rennes University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Dexamethasone 0.2 mg/kg

Dexamethasone 0.4 mg/kg

Ketoprofen 1 mg/kg

Arm Description

Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.2 mg / kg after general anesthesia induction and before surgery incision.

Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.4 mg / kg after general anesthesia induction and before surgery incision.

Single injection of ketoprofen (Medac ketoprofen ® 100 mg/4 ml injection ampoule solution) at 1 mg /kg after general anesthesia induction and before surgery incision.

Outcomes

Primary Outcome Measures

Maximum intensity of postoperative pain
Maximum intensity of postoperative pain assessed in PACU using the Faces Legs Activity Cry Consolability tool (FLACC, 0-10)

Secondary Outcome Measures

Pediatric Anesthesia Emergence Delirium Scale (PAEDS)
Pediatric Anesthesia Emergence Delirium Scale (PAEDS)
Intensity of postoperative pain
Intensity of postoperative pain assessed in ambulatory unit and at home one day after surgery. (FLACC, 0-10).
Rescue analgesic consumption
Rescue analgesic consumption in the PACU, ambulatory unit and at home.
Side effects
Side effects during hospitalization (PONV, postoperative bleeding) and in the first 24 hours post-surgery (PONV, fever, bleeding, behavior modification and sleep disorders).
Length of stay
Length of stay in ambulatory unit (time of possible discharge using Pediatric Post Anesthetic Discharge Scoring System and the actual time of discharge).
Parent's satisfaction
Parent's satisfaction on a four-point Likert scale

Full Information

First Posted
March 23, 2015
Last Updated
November 5, 2019
Sponsor
Rennes University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT02400047
Brief Title
Dexamethasone, Can it Replace Ketoprofen in the Strategy of Intraoperative Multimodal Analgesia in Paediatric Surgery ? A Prospective Randomized Double-blinded Study. DEXA OP
Acronym
DEXA OP
Official Title
Dexamethasone, Can it Replace Ketoprofen in the Strategy of Intraoperative Multimodal Analgesia in Paediatric Surgery ? A Prospective Randomized Double-blinded Study. DEXA OP
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
June 3, 2015 (Actual)
Primary Completion Date
July 18, 2019 (Actual)
Study Completion Date
July 18, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Postoperative pain and nausea-vomiting (PONV) are the first causes of failure in ambulatory care in pediatric surgery. Actually, the paracetamol/ketoprofen combination in intraoperative care is recommended for effective postoperative analgesia in children. However, intravenous ketoprofen doesn't have the marketing authorization for use in children less than 15 years old and its use is mainly justified by the absence of therapeutic alternatives. Recently, findings from published studies suggest that dexamethasone (DXM), which is actually recommended to prevent PONV for children "at risk", at a dose of 0.1mg/kg, would have analgesic properties above 0.15 mg/kg comparable to non-steroidal anti-inflammatories (NSAI). Main objective : To examine the effects of intraoperative DXM (0.2mg/kg and 0.4mg/kg) on the intensity of postoperative pain in the post-anaesthetic care unit (PACU) compared to ketoprofen (1mg/kg). Secondary objectives : To examine the effects of intraoperative DXM (0.2mg/kg and 0.4mg/kg) compared to ketoprofen (1mg/kg) on the anesthesia emergence delirium, the intensity of postoperative pain, the consumption of rescue analgesics and the side effects in the first 24 hours after surgery.
Detailed Description
Methodology : Non inferiority, phase III, therapeutic trial. Prospective, randomized double-blinded, monocentric study. Inclusion of 567 patients. Inclusion will be performed by the anesthesiologist, the day of surgery during the preoperative visit. Each patient will be randomised to receive intraoperative DXM (0.2mg/kg), DXM (0.4mg/kg) (max 20mg) or ketoprofen (1mg/kg) (max 100mg). The clinical data will be collected prospectively in an electronic database. If the hypothesis of non-inferiority is verified, it is planned to test the superiority of the hypothesis secondarily. Treatment : Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.2 mg / kg or 0.4 mg/kg or single injection of ketoprofen (Medac ketoprofen ® 100 mg/4 ml injection ampoule solution) at 1 mg /kg after general anesthesia induction and before surgery incision.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Nausea and Vomiting
Keywords
Paediatric surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
580 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dexamethasone 0.2 mg/kg
Arm Type
Experimental
Arm Description
Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.2 mg / kg after general anesthesia induction and before surgery incision.
Arm Title
Dexamethasone 0.4 mg/kg
Arm Type
Experimental
Arm Description
Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.4 mg / kg after general anesthesia induction and before surgery incision.
Arm Title
Ketoprofen 1 mg/kg
Arm Type
Active Comparator
Arm Description
Single injection of ketoprofen (Medac ketoprofen ® 100 mg/4 ml injection ampoule solution) at 1 mg /kg after general anesthesia induction and before surgery incision.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone 0.2 mg/kg
Intervention Description
Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.2 mg / kg after general anesthesia induction and before surgery incision.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone 0.4 mg/kg
Intervention Description
Single injection of DXM (Mylan Dexamethasone® 20 mg/5 ml or 4 mg/1 ml injection ampoule solution) at 0.4 mg / kg after general anesthesia induction and before surgery incision.
Intervention Type
Drug
Intervention Name(s)
Ketoprofen 1 mg/kg
Intervention Description
Single injection of ketoprofen (Medac ketoprofen ® 100 mg/4 ml injection ampoule solution) at 1 mg /kg after general anesthesia induction and before surgery incision.
Primary Outcome Measure Information:
Title
Maximum intensity of postoperative pain
Description
Maximum intensity of postoperative pain assessed in PACU using the Faces Legs Activity Cry Consolability tool (FLACC, 0-10)
Time Frame
1 hour
Secondary Outcome Measure Information:
Title
Pediatric Anesthesia Emergence Delirium Scale (PAEDS)
Description
Pediatric Anesthesia Emergence Delirium Scale (PAEDS)
Time Frame
24 hours
Title
Intensity of postoperative pain
Description
Intensity of postoperative pain assessed in ambulatory unit and at home one day after surgery. (FLACC, 0-10).
Time Frame
24 hours
Title
Rescue analgesic consumption
Description
Rescue analgesic consumption in the PACU, ambulatory unit and at home.
Time Frame
24 hours
Title
Side effects
Description
Side effects during hospitalization (PONV, postoperative bleeding) and in the first 24 hours post-surgery (PONV, fever, bleeding, behavior modification and sleep disorders).
Time Frame
24 hours
Title
Length of stay
Description
Length of stay in ambulatory unit (time of possible discharge using Pediatric Post Anesthetic Discharge Scoring System and the actual time of discharge).
Time Frame
24 hours
Title
Parent's satisfaction
Description
Parent's satisfaction on a four-point Likert scale
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children, aged 1 to 16 years Undergoing surgery (orchiopexy, inguinal hernia, circumcision, adenoidectomy, tonsillectomy or orthopedic act with osteosynthesis) Parental consent Exclusion Criteria: Contraindication to NSAI or DXM Hypersensitivity to ketoprofen, DXM, hypnovel or atarax Porphyria Long QT Syndrome Renal or hepatic impairment Corticosteroid consumption the week before surgery NSAI consumption within 48 hours before surgery IV induction for full stomach or myopathic patient. French language not spoken by parents. Simultaneous participation in biomedical research on health products
Facility Information:
Facility Name
Rennes University Hospital
City
Rennes
State/Province
Brittany
ZIP/Postal Code
35000
Country
France

12. IPD Sharing Statement

Learn more about this trial

Dexamethasone, Can it Replace Ketoprofen in the Strategy of Intraoperative Multimodal Analgesia in Paediatric Surgery ? A Prospective Randomized Double-blinded Study. DEXA OP

We'll reach out to this number within 24 hrs