- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00200564
Ketamine and Postoperative Analgesia in Children
October 22, 2007 updated by: Nantes University Hospital
The benefit of small doses of ketamine has been demonstrated for postoperative analgesia in adults but remains unproved in children.
The investigators' purpose is to evaluate the effects of continuous intravenous small doses of ketamine versus placebo to improve the quality of postoperative analgesia in children (6 months to 6 years of age).
Caudal anesthesia is performed for intraoperative analgesia and all children receive paracetamol, a non-steroidal anti-inflammatory and continuous intravenous nalbuphine.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
74
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Nantes, France, 44093
- Recruiting
- Nantes University Hospital
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Contact:
- Véronique Bazin, MD
- Phone Number: 00 33 2 40 08 35 47
- Email: veronique.bazin@chu-nantes.fr
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 months to 6 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children between 6 months to 6 years of age
- American Society of Anesthesiologists (ASA) I or II
- Undergoing elective surgery with intraoperative caudal analgesia
Exclusion Criteria:
- ASA III or IV
- Contraindication to caudal anesthesia
- Allergy to drugs used in the study
- Failure in caudal puncture
- Administration of morphine derivative
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Area under the curve of pain scores (CHEOPS) measured
Time Frame: every 2 hours during the first 24 hours after eyes open
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every 2 hours during the first 24 hours after eyes open
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Evaluation by the parents and nurses of the quality of analgesia with a visual analogue scale graded from 0 to 10
Time Frame: at the 24th hour
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at the 24th hour
|
|
Number of painful episodes requiring additional boluses of nalbuphine
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|
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Number of children requiring morphine after inefficiency of additional boluses of nalbuphine
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Percentage of children with side effects related to injection of ketamine
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Time to complete feeding
|
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Percentage of children with nausea or vomiting
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Véronique Bazin, MD, Nantes UH
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2004
Study Registration Dates
First Submitted
September 12, 2005
First Submitted That Met QC Criteria
September 12, 2005
First Posted (Estimate)
September 20, 2005
Study Record Updates
Last Update Posted (Estimate)
October 23, 2007
Last Update Submitted That Met QC Criteria
October 22, 2007
Last Verified
July 1, 2005
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Neurologic Manifestations
- Neurobehavioral Manifestations
- Perceptual Disorders
- Agnosia
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Central Nervous System Depressants
- Peripheral Nervous System Agents
- Analgesics
- Sensory System Agents
- Anesthetics, Dissociative
- Anesthetics, Intravenous
- Anesthetics, General
- Anesthetics
- Excitatory Amino Acid Antagonists
- Excitatory Amino Acid Agents
- Ketamine
Other Study ID Numbers
- BRD/03/12-H
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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