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Sponsored by: |
Institute of Child Health |
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Information provided by: | Institute of Child Health |
ClinicalTrials.gov Identifier: | NCT00231517 |
Randomised Double blind placebo controlled cross over design study of the efficacy of morphine for inflammatory pain in children with Epidermolysis Bullosa
Condition | Intervention | Phase |
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Epidermylosis Bullosa |
Drug: topical opiod Drug: morphine sulphate in intrasite gel |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Crossover Assignment, Efficacy Study |
Ages Eligible for Study: | 4 Years to 18 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
United Kingdom | |
Great Ormond Street Hospital and the Institute of Child health | |
London, United Kingdom, WC1N 1EH |
Principal Investigator: | Richard Howard, Prof | Institute of Child Health |
Study ID Numbers: | 01MH17 |
Study First Received: | October 3, 2005 |
Last Updated: | October 11, 2006 |
ClinicalTrials.gov Identifier: | NCT00231517 |
Health Authority: | United Kingdom: Research Ethics Committee |
Morphine Epidermolysis bullosa Skin Diseases, Vesiculobullous Genetic Diseases, Inborn Skin Diseases |
Skin Abnormalities Pain Epidermolysis Bullosa Congenital Abnormalities Skin Diseases, Genetic |
Sensory System Agents Therapeutic Uses Physiological Effects of Drugs Central Nervous System Depressants Narcotics |
Peripheral Nervous System Agents Analgesics Central Nervous System Agents Pharmacologic Actions Analgesics, Opioid |