Efficacy and Safety of FITpatch Compared to Standard Opioid Treatment in Cancer Pain (FT-015-IN)

Phase 3

Completed

• Conditions: Standard Opioid Analgesic Treatment of Cancer-related Chronic Pain.

• Registration Number: NCT00279344
• Lead Sponsor: Nycomed

Brief Summary

Primary objectives:

* To determine non-inferiority of FITpatch with regard to efficacy compared to standard opioid treatment

* To assess the safety of FITpatch compared to standard opioid treatment

Secondary objectives:

* To assess the intake of oral morphine as rescue analgesic to FITpatch compared to standard opioid treatment

* To assess Quality of life reported with FITpatch compared to standard opioid treatment

Detailed Description

Not available

Study Timeline

• Study Start: 2004-09
• Study First Submitted: 2005-12-14
• Study First Submitted QC: 2006-01-17
• Study First Posted: 2006-01-19
• Study Completion: 2007-08
• Status Verified: 2012-05
• Last Update Submitted: 2012-05-04
• Last Update Posted: 2012-05-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 220

Inclusion Criteria

Subjects that have insufficiently treated, cancer-related chronic pain that requires long-term treatment with an opioid at Step 3 on the WHO Ladder, and with Karnofsky performance status above 50.

1. Subject informed consent given.
2. Aged between 18 and 75 years, and for female subjects a proven negative pregnancy test and adequate contraception.
3. No significant skin lesions on relevant surfaces on the body or diffuse skin diseases.
4. No impaired respiratory function nor neurological or psychiatric impairment.
5. No known abuse of drug, narcotic or alcohol.
6. Not pregnant or nursing.
7. Not hypersensitive/allergic to fentanyl or morphine.
8. No head injury, primary brain tumor, increased intracranial pressure or impaired consciousness.
9. Not participating in other clinical trials.

Exclusion Criteria

All exclusion criteria must be answered No for a patient to participate in the trial.

1. Does the patient have significant skin lesions on the upper arms/flat surface of the upper torso or diffuse skin disease (psoriasis or eczema) that preclude application of fentanyl patches?
2. Does the patient have a known abuse of drug, narcotic or alcohol?
3. Is the patient pregnant or nursing?
4. Has the patient neurological or mental impairment that may compromise data collection?
5. Is the patient hypersensitive/allergic to fentanyl or morphine or any of the ingredients in the trial medication?
6. Has the patient any major head injury, primary brain tumour, increased intracranial pressure or impaired consciousness?
7. Does the patient participate in other clinical with other investigational drugs or investigation al medical devices or has been participating in such a trial for the past 30 days?

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Primary:
To determine non-inferiority of FITpatch with regard to efficacy compared to standard opioid treatment and to assess the safety of FITpatch compared to standard opioid treatment

Secondary Outcome Measures

Name	Time	Method
Secondary:
To assess the intake of oral morphine as rescue analgesic to FITpatch compared to standard opioid treatment and to assess Quality of life reported with FITpatch compared to standard opioid treatment