WHO ICTRP trial

A Comparison of Remifentanil Patient-Controlled Analgesia vs. Oral Morphine…

EUCTR2008-007322-19-GB · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2008-007322-19-GB
Public title A Comparison of Remifentanil Patient-Controlled Analgesia vs. Oral Morphine Analgesia for Dressing Changes in Burns Patients.
Scientific title A Comparison of Remifentanil Patient-Controlled Analgesia vs. Oral Morphine Analgesia for Dressing Changes in Burns Patients.
Primary sponsor Queen Victoria Hospital NHS Foundation Trust
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes
Countries United Kingdom
Conditions Pain experienced by patients with pre-existing burns presenting to the burns outpatients unit requiring two or more dressing changes
Interventions Trade Name: Remifentanil Product Name: Remifentanil Pharmaceutical Form: Powder for solution for infusion Trade Name: Oramorph Product Name: Oramorph Pharmaceutical Form: Oral solution
Registration date Nov 23, 2010
Target size 58
Secondary IDs RPC190
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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