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NCT00000318 · ClinicalTrials.gov registry record · Phase 2

Buprenorphine Maintenance Dose Schedule and Treatment Setting - 1

A Phase 2 study of Substance-Related Disorders and Opioid-Related Disorders, sponsored by National Institute on Drug Abuse (NIDA).

Completed
Registry status
Phase 2
Development phase
202
Enrollment target
1
Study location

NCT00000318 is a Phase 2 study of Substance-Related Disorders and Opioid-Related Disorders that has completed, run by National Institute on Drug Abuse (NIDA). The registered enrollment target is 202 participants, below the 1,518-participant average among 58 other Substance-Related Disorders trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00000318, a Phase 2 study of Substance-Related Disorders and Opioid-Related Disorders, has completed, sponsored by National Institute on Drug Abuse (NIDA).

COMPLETED
Registry status
Phase 2
Development phase
202 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to assess optimal dosage of buprenorphine on a thrice weekly schedule in a pilot clinical trial.

Interventions

  • DRUG Buprenorphine

Study Locations (1)

Connecticut

  • APT Residential Services Division - New Haven

Trial Details

FieldValue
Enrollment Target 202 participants
Start Date 1994-12
Est. Completion 2007-08
Phase Phase 2

What the Registry Record Tells You About NCT00000318

The ClinicalTrials.gov registry entry for NCT00000318 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 202 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,518-participant average among 58 other Substance-Related Disorders trials with a reported enrollment target (87% lower). The listed sponsor is National Institute on Drug Abuse (NIDA), which has 335 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Substance-Related Disorders appearing as the primary indexed condition, and to 1 intervention - of which Buprenorphine is the first listed.

NCT00000318 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT00000318 about?

NCT00000318 is a clinical study titled "Buprenorphine Maintenance Dose Schedule and Treatment Setting - 1". The purpose of this study is to assess optimal dosage of buprenorphine on a thrice weekly schedule in a pilot clinical trial.

What is the current status of trial NCT00000318?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 202 participants. The study started on 1994-12. Estimated completion is 2007-08.

What conditions does trial NCT00000318 study?

This clinical trial studies the following conditions: Substance-Related Disorders, Opioid-Related Disorders.

What interventions are being tested in trial NCT00000318?

The interventions under investigation include: Buprenorphine (DRUG).

Who is sponsoring clinical trial NCT00000318?

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

Where is trial NCT00000318 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.