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

NCT00044083 · ClinicalTrials.gov registry record · Phase 2

Clinical Trial of Tolcapone for Cognition in Schizophrenia

A Phase 2 study, sponsored by National Institute of Mental Health (NIMH).

Terminated
Registry status
Phase 2
Development phase
210
Enrollment target

NCT00044083: Clinical Trial Phase 2 study, sponsored by National Institute of Mental Health (NIMH).

NCT00044083 is a Phase 2 study that was terminated before completion, run by National Institute of Mental Health (NIMH). The registered enrollment target is 210 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00044083, a Phase 2 study, was terminated before completion, sponsored by National Institute of Mental Health (NIMH).

TERMINATED
Registry status
Phase 2
Development phase
210 participants
Enrollment target

Study Summary

This study will evaluate whether Tolcapone improves cognition in healthy volunteers as well as patients with schizophrenia. Talcapone is a drug that has been FDA approved for Attention Deficit Disorder and allegedly increase the amount of the neurotransmitter dopamine in the frontal cortex of the brain. ...

Primary Outcome

Working Memory was measured in HVs and patients with schizophrenia after a 7-day treatment with Tolcapone or placebo in a double-blind, cross-over fashion. The working memory was quantified by taking the number of trials entered correctly divided by the total number of trials multiplied by 100. Values range from 0 to 100. Zero indicates the poorest performance while 100 indicates perfect performance.

Interventions

  • OTHER Placebo
  • DRUG Tolcapone

Trial Details

FieldValue
Enrollment Target 210 participants
Start Date 2002-08
Est. Completion 2015-12
Phase Phase 2

Why NCT00044083 stopped before completion

NCT00044083 is an interventional study that assigns participants to a tested intervention. The registered 210 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (58% higher).

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

NCT00044083 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00044083 about?

NCT00044083 is a clinical study titled "Clinical Trial of Tolcapone for Cognition in Schizophrenia". This study will evaluate whether Tolcapone improves cognition in healthy volunteers as well as patients with schizophrenia. Talcapone is a drug that has been FDA approved for Attention Deficit Disorder and allegedly increase the amount of the neurotransmitter dopamine in the frontal cortex of the br...

What is the current status of trial NCT00044083?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 210 participants. The study started on 2002-08. Estimated completion is 2015-12.

What interventions are being tested in trial NCT00044083?

The interventions under investigation include: Placebo (OTHER), Tolcapone (DRUG).

Who is sponsoring clinical trial NCT00044083?

This trial is sponsored by National Institute of Mental Health (NIMH), which has 343 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00044083's enrollment target sits among peer trials

210 290th of 2000 higher than 1,707 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02665923 · 210 participants

    Gastric Emptying in Neonates and Infants After Formula Feeding

  • NCT03322891 · 210 participants · NA

    Improving Health Literacy in African-American Prostate Cancer Patients

  • NCT03544489 · 210 participants · Phase 2

    Effectiveness of Exercise After an ICD

  • NCT04408430 · 210 participants · NA

    The MITRAL II Pivotal Trial (Mitral Implantation of TRAnscatheter vaLves).

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00044083, the US trial registry maintained by the National Library of Medicine. NCT00044083 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.