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NCT02372591 · ClinicalTrials.gov registry record · Phase 1

Study of the Treatment of Experimental Pain in Buprenorphine Maintained Persons With Chronic Musculoskeletal Pain

A Phase 1 study, sponsored by Johns Hopkins University.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT02372591: Completed Phase 1 study, sponsored by Johns Hopkins University.

NCT02372591 is a Phase 1 study that has completed, run by Johns Hopkins University. The registered enrollment target is 14 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02372591, a Phase 1 study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

Pain is very common in persons with a history of addiction, but few studies have examined the best treatment of pain in this population. This is a study to determine the pain relief provided by intravenous hydromorphone (Dilaudid) or buprenorphine given to persons maintained on stable doses of methadone or buprenorphine who have chronic musculoskeletal pain. Experimental sessions will require overnight stays on a residential research unit. In these sessions, persons will be exposed to standard experimental pain techniques at baseline and then rate the relief (if any) provided by the study medication when exposed to the same techniques. Persons will be asked to participate in 3 sessions, each separated by at least 7 days.

Interventions

  • DRUG Placebo
  • DRUG Hydromorphone
  • DRUG Buprenorphine

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2015-08
Est. Completion 2017-06
Phase Phase 1

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT02372591

The ClinicalTrials.gov registry entry for NCT02372591 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 14 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT02372591 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02372591 about?

NCT02372591 is a clinical study titled "Study of the Treatment of Experimental Pain in Buprenorphine Maintained Persons With Chronic Musculoskeletal Pain". Pain is very common in persons with a history of addiction, but few studies have examined the best treatment of pain in this population. This is a study to determine the pain relief provided by intravenous hydromorphone (Dilaudid) or buprenorphine given to persons maintained on stable doses of metha...

What is the current status of trial NCT02372591?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2015-08. Estimated completion is 2017-06.

What interventions are being tested in trial NCT02372591?

The interventions under investigation include: Placebo (DRUG), Hydromorphone (DRUG), Buprenorphine (DRUG).

Who is sponsoring clinical trial NCT02372591?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.