Overview
Efficacy and Safety of FITpatch Compared to Standard Opioid Treatment in Cancer Pain (FT-015-IN)
Status:
Completed
Completed
Trial end date:
2007-08-01
2007-08-01
Target enrollment:
0
0
Participant gender:
All
All
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 treatmentPhase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
NycomedTreatments:
Fentanyl
Criteria
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?