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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Study Classification

INTERVENTIONAL

Brief Summary

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

Detailed Description

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Conditions

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Epidermylosis Bullosa

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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topical opiod

Intervention Type DRUG

morphine sulphate in intrasite gel

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* children under 18 years epidermolysis wounds requiring dressing changes

Minimum Eligible Age

4 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Richard Howard, Prof

Role: PRINCIPAL_INVESTIGATOR

Institute of Child Health

Locations

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Great Ormond Street Hospital and the Institute of Child health

London, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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01MH17

Identifier Type: -

Identifier Source: org_study_id