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Randomised Double Blind Placebo Controlled Cross Over Design of the Efficacy of Topical Morphine for Inflammatory Pain in Children With Epidermolysis Bullosa

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ClinicalTrials.gov Identifier: NCT00231517
Recruitment Status : Completed
First Posted : October 4, 2005
Last Update Posted : October 12, 2006
Sponsor:
Information provided by:
Institute of Child Health

Study Description
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Brief Summary:
Randomised Double blind placebo controlled cross over design study of the efficacy of morphine for inflammatory pain in children with Epidermolysis Bullosa

Condition or disease Intervention/treatment Phase
Epidermylosis Bullosa Drug: topical opiod Drug: morphine sulphate in intrasite gel Phase 4

Study Design
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Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double
Primary Purpose: Treatment

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Arms and Interventions
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Outcome Measures
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Eligibility Criteria
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Ages Eligible for Study:   4 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • children under 18 years epidermolysis wounds requiring dressing changes
Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00231517


Locations
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United Kingdom
Great Ormond Street Hospital and the Institute of Child health
London, United Kingdom, WC1N 1EH
Sponsors and Collaborators
Institute of Child Health
Investigators
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Principal Investigator: Richard Howard, Prof Institute of Child Health
More Information
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ClinicalTrials.gov Identifier: NCT00231517    
Other Study ID Numbers: 01MH17
First Posted: October 4, 2005    Key Record Dates
Last Update Posted: October 12, 2006
Last Verified: October 2005
Additional relevant MeSH terms:
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Morphine
Analgesics, Opioid
Narcotics
Central Nervous System Depressants
 Physiological Effects of Drugs
Analgesics
Sensory System Agents
Peripheral Nervous System Agents