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NCT00177463 · ClinicalTrials.gov registry record · NA

L-Carnosine for Bipolar I Disorder

A NA study, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
47
Enrollment target

NCT00177463: Completed NA study, sponsored by University of Pittsburgh.

NCT00177463 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 47 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00177463, a NA study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
47 participants
Enrollment target

Study Summary

Our hypothesis is that oral L-carnosine treatment (as compared with placebo) will enhance cognitive abilities (specifically: measures of attention, executive function, working memory, visuospatial ability and language) in persons with bipolar disorder. Secondarily, we hypothesize there will be secondary improvements in positive, negative and mood symptoms with L-carnosine treatment. We aim to test these hypotheses by conducting a randomized, placebo controlled, add on treatment trial of L-carnosine (added to existing antipsychotic treatment) on 48 recruited subjects with DSM IV TR bipolar disorder for a period of 12 weeks. Measures of cognition, and psychopathology will be utilized for evaluating primary and secondary outcomes, along with safety assessments.

Interventions

  • DRUG L-carnosine

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2004-09
Est. Completion 2007-12
Phase NA
University of Pittsburgh

1,238 total trials

What the finished NCT00177463 record still lists

NCT00177463 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which L-carnosine is the first listed.

NCT00177463 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00177463 about?

NCT00177463 is a clinical study titled "L-Carnosine for Bipolar I Disorder". Our hypothesis is that oral L-carnosine treatment (as compared with placebo) will enhance cognitive abilities (specifically: measures of attention, executive function, working memory, visuospatial ability and language) in persons with bipolar disorder. Secondarily, we hypothesize there will be secon...

What is the current status of trial NCT00177463?

This trial is currently completed. It is a NA study. The enrollment target is 47 participants. The study started on 2004-09. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00177463?

The interventions under investigation include: L-carnosine (DRUG).

Who is sponsoring clinical trial NCT00177463?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00177463's enrollment target sits among peer trials

47 1400th of 2000 higher than 599 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT00177463, the US trial registry maintained by the National Library of Medicine. NCT00177463 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.