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| Sponsored by: |
Janssen Cilag S.A.S. |
|---|---|
| Information provided by: | Janssen Cilag S.A.S. |
| ClinicalTrials.gov Identifier: | NCT00236327 |
Purpose
The purpose of this study is to determine the safety and efficacy of pain control by fentanyl, administered via adhesive skin patches, at doses of 25 to 100 micrograms per hour in 80 out-patients with intense chronic cancer pain. Higher doses are allowed by permission of the investigator and rescue oral morphine medication is allowed.
| Condition | Intervention | Phase |
|---|---|---|
|
Pain |
Drug: fentanyl |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | Evaluation of the Efficacy and Safety of Transdermal Fentanyl in Patients Suffering From Chronic Cancer Pain in an Ambulatory Setting |
| Estimated Enrollment: | 80 |
| Study Start Date: | June 2003 |
| Estimated Study Completion Date: | May 2004 |
Patients with cancer pain are frequently under-medicated with morphine. This is a 56-day open-label study of the efficacy and safety of self-administered fentanyl skin patches for cancer pain control in patients in the home-care setting not previously using morphine. The first 15 days of the study are for dose stabilization and the rest of the study assesses pain control and quality of life at stable doses of medication. The dose is determined by the patient with oversight by the investigator, and rescue oral morphine medication can be used when necessary. The patient records all medication use in a diary and fills out questionnaires concerning pain control, intestinal function (constipation) and overall quality of life. The hypothesis is that patients will be able to control their cancer pain by self-administering transdermal fentanyl at home and that they will well tolerate the medication.
Individualized doses, with a target dose of 25 to 100 micrograms per hour of fentanyl for 56 days via skin patches applied every 3 days to deliver 25 to 100 micrograms of fentanyl per hour per patch; oral morphine as rescue medication for pain.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria: - Less than a month of opioid treatment over the past 3 months - Proven cancer and chronic stable, cancer-related pain - Pain control medication (aside from opioids) at the maximum authorized dose in the 24-hours preceding the first study visit - A pain score of at least 4 on the VAS scale and pain that justifies intervention by opium-derived drugs in the opinion of the investigator
Exclusion Criteria: - Liver or kidney problems - Previous heart, lung or nervous disorders - Allergy to fentanyl - Skin condition that might interfere with absorption of the fentanyl through the skin - Surgery or chemotherapy in the month preceding the study or scheduled during the 56 days of the study - History of substance abuse.
Contacts and Locations More Information
| Study ID Numbers: | CR002920 |
| Study First Received: | October 7, 2005 |
| Last Updated: | December 16, 2005 |
| ClinicalTrials.gov Identifier: | NCT00236327 |
| Health Authority: | France: Ministry of Health |
|
Opioid analgesia Cancer pain Patient-controlled analgesia Analgesia |
Pain Fentanyl Transdermal fentanyl |
|
Fentanyl Pain |
|
Anesthetics, Intravenous Physiological Effects of Drugs Central Nervous System Depressants Anesthetics Narcotics Pharmacologic Actions Adjuvants, Anesthesia |
Sensory System Agents Anesthetics, General Therapeutic Uses Analgesics Peripheral Nervous System Agents Central Nervous System Agents Analgesics, Opioid |
