Efficacy and Safety of Hydromorphone Hydrochloride Extended-Release Compared to Placebo in Subjects With Persistent Pain
NCT00365898 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 380
Last updated 2006-08-18
Summary
The objective of this study is to assess the efficacy and safety of 8 mg Hydromorphone Hydrochloride Extended-Release.
Conditions
- Chronic Non-Malignant Pain
Interventions
- DRUG
-
Hydromorphone Hydrochloride Extended-Release
Sponsors & Collaborators
-
Purdue Pharma LP
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-07-31
- Completion
- 2005-07-31
Countries
- United States
Study Locations
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