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| Sponsor: | Institute of Child Health |
|---|---|
| Information provided by: | Institute of Child Health |
| ClinicalTrials.gov Identifier: | NCT00231517 |
Purpose
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 |
|---|---|---|
|
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 |
Eligibility| Ages Eligible for Study: | 4 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations| 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 |
More Information
| Study ID Numbers: | 01MH17 |
| Study First Received: | October 3, 2005 |
| Last Updated: | October 11, 2006 |
| ClinicalTrials.gov Identifier: | NCT00231517 History of Changes |
| Health Authority: | United Kingdom: Research Ethics Committee |
|
Morphine Skin Diseases Skin Diseases, Vesiculobullous Physiological Effects of Drugs Skin Abnormalities Central Nervous System Depressants Narcotics Epidermolysis Bullosa Pharmacologic Actions |
Genetic Diseases, Inborn Sensory System Agents Therapeutic Uses Analgesics Peripheral Nervous System Agents Congenital Abnormalities Central Nervous System Agents Skin Diseases, Genetic Analgesics, Opioid |