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

RECRUITING

Substance Abuse Pre-Treatment Screening Study

NCT00439049 · View on ClinicalTrials.gov ↗

Study Summary

The overarching goal of this project is to have a consolidated consent and evaluation procedure that will lead potential subjects to the most appropriate clinical trial or human laboratory study (and its consent process) for their presenting concerns or interests. A second purpose is to have a consolidated intake data base on which secondary analyses can be conducted.

Interventions

  • DRUG Naltrexone
  • DRUG modafinil
  • DRUG d-amphetamine
  • DRUG L-Dopa

Study Locations (1)

Texas

  • University of Texas Medical School- Houston, Dept. of Psychiatry Mental Sciences Institute — Houston

Trial Details

FieldValue
Enrollment Target 7,500 participants
Start Date 2005-10
Est. Completion 2026-06

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00439049

The ClinicalTrials.gov registry entry for NCT00439049 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 7,500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 811 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Substance Abuse appearing as the primary indexed condition, and to 4 interventions — of which Naltrexone is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00439049 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00439049 about?

NCT00439049 is a clinical study titled "Substance Abuse Pre-Treatment Screening Study". The overarching goal of this project is to have a consolidated consent and evaluation procedure that will lead potential subjects to the most appropriate clinical trial or human laboratory study (and its consent process) for their presenting concerns or interests. A second purpose is to have a conso...

What is the current status of trial NCT00439049?

This trial is currently recruiting. The enrollment target is 7,500 participants. The study started on 2005-10. Estimated completion is 2026-06.

What conditions does trial NCT00439049 study?

This clinical trial studies the following conditions: Substance Abuse, Alcohol Dependence, Cocaine Dependence, Opiate Dependence, Cocaine Abuse. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00439049?

The interventions under investigation include: Naltrexone (DRUG), modafinil (DRUG), d-amphetamine (DRUG), L-Dopa (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00439049?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 811 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00439049 being conducted?

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

Related

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