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TERMINATED
NCT01841931
PHASE4

Buprenorphine Treatment: A Safe Alternative for Opioid Dependent Pain Patients

Sponsor: Theresa Jacob, PhD, MPH

View on ClinicalTrials.gov

Summary

The purpose of this study is to examine whether buprenorphine can be at least as effective as other opioid medications in relieving chronic pain in patients who suffer from dependence on their opioid medications, while patients simultaneously experience progressive decline of pain along with absence of opioid withdrawal symptoms and improved quality of life.

Official title: Buprenorphine Tx:A Safe Alternative for Opioid Dependent Pain Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

4

Start Date

2013-02

Completion Date

2013-08

Last Updated

2026-05-08

Healthy Volunteers

No

Interventions

DRUG

Buprenorphine/Naloxone

Sublingual buprenorphine/naloxone taken in a 3 day induction, with a final daily dose (up to 32 mg depending on the subject) taken daily, as prescribed by the study psychiatrist. Subjects will continue buprenorphine for study duration (6 months).

Locations (1)

Maimonides Medical Center

Brooklyn, New York, United States