Status:
TERMINATED
An Observational, Non-Interventional Trial to Assess Patient Satisfaction and Safety of Subsys™ Spray.
Lead Sponsor:
International Clinical Research Institute
Conditions:
Breakthrough Pain
Eligibility:
All Genders
18+ years
Brief Summary
Chronic pain patients who experience breakthrough pain in the background of controlled persistent pain with opioids will be followed for 3 months in order to assess the safety and titration trends in ...
Detailed Description
Approximately 100 subjects across 10 centers throughout the United States will be enrolled into the study. Subjects who are currently taking Actiq® for their breakthrough pain and will be discontinued...
Eligibility Criteria
Inclusion
- Patients ≥ 18 years of age.
- Subjects who are experiencing 1-4 episodes of break through pain per day in spite of optimized background analgesia and who have taken at least 60 mg/day of morphine (or equivalent analgesic) for at least 7 days.
- Who are currently using Actiq® for their breakthrough pain and are being discontinued due to lack of efficacy, side effects, patient dissatisfaction or prescriber dissatisfaction with treatment.
- Are able to follow and complete all necessary study procedures.
- Are willing and able to give written informed consent before participating in the study.
- Enrolled in the class wide REMS as verified by the study personnel.
Exclusion
- Subjects who are not opioid tolerant.
- Using a rapid onset opioid other than Actiq® to manage their breakthrough pain.
- Have physical abnormalities of the floor of the mouth that could affect absorption as determined by investigator.
- Are subjects with uncontrolled or rapidly escalating pain.
- Are subjects with a history of alcohol or substance abuse within the last 3 years.
- Have a clinically significant medical history (past or present) of any disease that would compromise the study or the well-being of the subject.
- Are subjects who have participated in another clinical trial with an analgesic within the last month.
- Are female subjects with a positive pregnancy test or who are currently lactating.
- Are subjects who are taking medications that are known inhibitors of the CYP3A4 isozyme, such as ketoconazole.
- Are subjects who have taken a monoamine inhibitor within 14 days before a dose of study medication.
- Opioid being used for chronic migraine or acute pain.
- Are subjects who are unsuitable for inclusion for any other reason, in the opinion of the investigator.
Key Trial Info
Start Date :
April 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2014
Estimated Enrollment :
4 Patients enrolled
Trial Details
Trial ID
NCT01901718
Start Date
April 1 2013
End Date
January 1 2014
Last Update
September 4 2014
Active Locations (1)
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1
International Clinical Research Institute
Overland Park, Kansas, United States, 66210