New hope for pain relief without addiction: buprenorphine study
NCT ID NCT01841931
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether buprenorphine can effectively treat chronic pain in people who are dependent on opioid painkillers, while also reducing withdrawal symptoms and improving quality of life. It involved 4 adults with opioid dependence and chronic pain. The approach was to switch them from their current opioids to buprenorphine over 3 days and monitor pain and withdrawal. The study was terminated early, so results are limited.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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4 people
The number who actually took part.
- Started
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Feb 2013
- Finished
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Aug 2013
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Meets DSM criteria for opioid dependence (or opioid use disorder when DSM 5 is in use) * Has received opioid therapy for at least 90 days * Has opioid dependence as assessed by a Maimonides psychiatrist Exclusion Criteria: * Scheduled for major surgery during study duration * Predicted life expectancy \< 1 year * Plan to cease habitation in greater New York area within 6 months * Risks for buprenorphine outweigh potential benefit, as determined by the PI * Lacks sufficient fluency in English to understand the study protocol, answer survey questions or give informed consent * Pregnant women
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Maimonides Medical Center
Brooklyn, New York, 11219, United States
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Other studies related to the condition(s) this trial covers.
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