Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02927236 · ClinicalTrials.gov registry record · NA

Theta-Burst Stimulation as a Treatment for Reducing Cocaine Use

A NA study, sponsored by National Institute on Drug Abuse (NIDA).

Terminated
Registry status
NA
Development phase
45
Enrollment target

NCT02927236 is a NA study that was terminated before completion, run by National Institute on Drug Abuse (NIDA). The registered enrollment target is 45 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02927236, a NA study, was terminated before completion, sponsored by National Institute on Drug Abuse (NIDA).

TERMINATED
Registry status
NA
Development phase
45 participants
Enrollment target

Study Summary

Objective: The goal of this clinical trial is to assess the tolerability of an accelerated intermittent theta burst stimulation (iTBS), a form of transcranial magnetic stimulation, intervention in participants with cocaine use disorder and then to determine if the intervention changes brain circuits related to cocaine use disorder and whether these changes relate to clinical outcomes. The main questions it aims to answer are: * Can individuals with cocaine use disorder tolerate accelerated iTBS (3 treatments per day for 10 days) (Pilot study)? * Does iTBS (compared to sham iTBS) alter brain circuits related to cocaine use disorder (Expanded feasibility study)? Researchers will compare individuals with cocaine use disorder to those without cocaine use disorder to identify differences at baseline, compare effects of the first day of iTBS treatment, and see if changes after treatment align brain circuits in those with cocaine use disorder more closely to patterns seen in those without cocaine use disorder. Participants will: * Undergo 10 days of iTBS treatment and two follow-up visits (1 week and 4 weeks after treatment) and complete questionnaires throughout to assess tolerability and drug use (Pilot study). * Participants with cocaine use disorder will complete a characterization phase with questionnaires, two fMRI scans and a trial session of iTBS (sham or active) before the treatment phase (Expanded feasibility study).

Interventions

  • DEVICE Transcranial magnetic stimulation (TMS)

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2017-02-13
Est. Completion 2023-10-30
Phase NA

What the Registry Record Tells You About NCT02927236

The ClinicalTrials.gov registry entry for NCT02927236 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute on Drug Abuse (NIDA), which has 335 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Transcranial magnetic stimulation (TMS) is the first listed.

NCT02927236 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02927236 about?

NCT02927236 is a clinical study titled "Theta-Burst Stimulation as a Treatment for Reducing Cocaine Use". Objective: The goal of this clinical trial is to assess the tolerability of an accelerated intermittent theta burst stimulation (iTBS), a form of transcranial magnetic stimulation, intervention in participants with cocaine use disorder and then to determine if the intervention changes brain circuits...

What is the current status of trial NCT02927236?

This trial is currently terminated. It is a NA study. The enrollment target is 45 participants. The study started on 2017-02-13. Estimated completion is 2023-10-30.

What interventions are being tested in trial NCT02927236?

The interventions under investigation include: Transcranial magnetic stimulation (TMS) (DEVICE).

Who is sponsoring clinical trial NCT02927236?

This trial is sponsored by National Institute on Drug Abuse (NIDA), which has 335 total clinical trials registered on ClinicalTrials.gov.

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

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, or report a data error.