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NCT03521960 · ClinicalTrials.gov registry record · Phase 1

Buspirone for Opioid Tapering

A Phase 1 study, sponsored by Johns Hopkins University.

Completed
Registry status
Phase 1
Development phase
18
Enrollment target

NCT03521960: Completed Phase 1 study, sponsored by Johns Hopkins University.

NCT03521960 is a Phase 1 study that has completed, run by Johns Hopkins University. The registered enrollment target is 18 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03521960, a Phase 1 study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
Phase 1
Development phase
18 participants
Enrollment target

Study Summary

This is a pilot study to collect preliminary data to support a grant application. The goal of the study is to evaluate whether the Food and Drug Administration (FDA)-approved and generically-available medication buspirone reduces symptoms of opioid withdrawal among patients undergoing a clinically-indicated and supervised taper from their opioid pain medications. This is premised on strong preclinical scientific support but has not yet be well-examined in humans.

Primary Outcome

Final day on which participant is enrolled in the clinic

Interventions

  • DRUG Placebo oral capsule
  • DRUG Buspirone oral capsule

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2018-05-30
Est. Completion 2020-06-30
Phase Phase 1
Johns Hopkins University

1,448 total trials

What the finished NCT03521960 record still lists

NCT03521960 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo oral capsule is the first listed.

NCT03521960 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03521960 about?

NCT03521960 is a clinical study titled "Buspirone for Opioid Tapering". This is a pilot study to collect preliminary data to support a grant application. The goal of the study is to evaluate whether the Food and Drug Administration (FDA)-approved and generically-available medication buspirone reduces symptoms of opioid withdrawal among patients undergoing a clinically-i...

What is the current status of trial NCT03521960?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2018-05-30. Estimated completion is 2020-06-30.

What interventions are being tested in trial NCT03521960?

The interventions under investigation include: Placebo oral capsule (DRUG), Buspirone oral capsule (DRUG).

Who is sponsoring clinical trial NCT03521960?

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

How this trial's enrollment target compares

Where NCT03521960's enrollment target sits among peer trials

18 1720th of 2000 higher than 216 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03521960, the US trial registry maintained by the National Library of Medicine. NCT03521960 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.