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COMPLETED NA

Safety and Effectiveness of Giving Lamisil to HIV-Positive Subjects With Thrush Who Have Not Responded to Fluconazole Treatment

NCT00002394 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to see if it is safe and effective to give Lamisil to HIV-positive patients with thrush (a fungal infection) that has not responded to fluconazole.

Interventions

  • DRUG Terbinafine hydrochloride

Study Locations (9)

Florida

  • Therafirst Med Ctr — Fort Lauderdale
  • Associates in Research — Fort Myers
  • Clireco Inc — Tamarac
  • Infectious Diseases Research Inc — Tampa

Illinois

  • Northwestern Univ / Division of Infectious Disease — Chicago

New Jersey

  • Saint Michaels Med Ctr / Infectious Disease Resch Dpt — Newark

New York

  • St Vincents Hosp / Clinical Research Program — New York

Texas

  • Univ of Texas Med Branch — Galveston

Virginia

  • Hampton Roads Med Specialists — Hampton

Trial Details

FieldValue
Enrollment Target 30 participants
Phase NA

Sponsor

Novartis

60 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00002394

The ClinicalTrials.gov registry entry for NCT00002394 describes a study currently listed as completed. It is categorized as NA, 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis, which has 60 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with HIV Infections appearing as the primary indexed condition, and to 1 intervention — of which Terbinafine hydrochloride 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: NCT00002394 reports 9 study locations spanning 6 distinct geographic areas — top geographies include Florida, Illinois, New Jersey. 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 NCT00002394 about?

NCT00002394 is a clinical study titled "Safety and Effectiveness of Giving Lamisil to HIV-Positive Subjects With Thrush Who Have Not Responded to Fluconazole Treatment". The purpose of this study is to see if it is safe and effective to give Lamisil to HIV-positive patients with thrush (a fungal infection) that has not responded to fluconazole.

What is the current status of trial NCT00002394?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants.

What conditions does trial NCT00002394 study?

This clinical trial studies the following conditions: HIV Infections, Candidiasis, Oral. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00002394?

The interventions under investigation include: Terbinafine hydrochloride (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00002394?

This trial is sponsored by Novartis, which has 60 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00002394 being conducted?

This trial has 9 study locations across Florida, Illinois, New Jersey, New York, 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