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Spots Global Cancer Trial Database for Bioavailability and Effectiveness of Transdermally Administered Morphine

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Trial Identification

Brief Title: Bioavailability and Effectiveness of Transdermally Administered Morphine

Official Title: Bioavailability and Effectiveness of Transdermally Administered Morphine

Study ID: NCT00125684

Conditions

Cancer
Pain

Interventions

morphine

Study Description

Brief Summary: Patients will participate in two arms of the trial, one in which morphine will be administered transdermally, and, after a 3 day wash out period, one in which morphine will be administered subcutaneously.

Detailed Description: Patients will participate in two arms of the trial, one in which morphine will be administered transdermally, and, after a 3 day wash out period, one in which morphine will be administered subcutaneously. Blood draws will be done after both dosing methods in order to compare blood levels of morphine by the different routes.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Tom Baker Cancer Centre, Calgary, Alberta, Canada

Contact Details

Name: Neil Hagen

Affiliation: Alberta Cancerboard

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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