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Efficacy and Safety Study of Fentanyl Transdermal (Fentanest®)

2014-08-27 03:20:02 | BioPortfolio

Summary

Eligible patients who agree to participate will migrate from oral opioids to transdermal patches and be followed for four weeks. Oral morphine will be provided as pain rescue medication. The patients will inform the adverse events and rescue medication consumption. The number of Fentanest® patches will be adjusted every visit aiming to reduce the rescue medication consumption and adverse events to a minimum. The WHO-QOL- bref (quality of life questionary) will be filled before and after the use of Fentanest®. Patients showing benefit are eligible to a 3 weeks compassionate study.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Pain

Intervention

Fentanyl Transdermal

Location

Hospital Universitario da Universidade Federal do Maranhao
Sao Luis
Maranhao
Brazil
65020-070

Status

Withdrawn

Source

Cristália Produtos Químicos Farmacêuticos Ltda.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:20:02-0400

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