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

NCT00588731 · ClinicalTrials.gov registry record · Phase 2

Cannabidiol Treatment of Cognitive Dysfunction in Schizophrenia

A Phase 2 study, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
41
Enrollment target

NCT00588731: Completed Phase 2 study, sponsored by Yale University.

NCT00588731 is a Phase 2 study that has completed, run by Yale University. The registered enrollment target is 41 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00588731, a Phase 2 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
41 participants
Enrollment target

Study Summary

This study is a six-week, randomized, placebo-controlled, fixed dose trial comparing cannabidiol Vs. placebo added to a stable dose of antipsychotic medications in patients diagnosed with schizophrenia.

Primary Outcome

Verbal short term memory is measured through the Hopkins Verbal Learning Test. Each trial has a max total score of 12 (range of 0-12), and the max total score for all three trials is 36 (range of 0-36). However, the data listed below is reported in the form of a t-score, with a higher score representing better verbal learning. These t-score values are normalizing the scores to populations, comparing them to a representative sample, with a mean of 50.

Interventions

  • DRUG Placebo
  • DRUG Cannabidiol

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2009-02
Est. Completion 2013-12
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT00588731 record still lists

NCT00588731 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower).

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

NCT00588731 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00588731 about?

NCT00588731 is a clinical study titled "Cannabidiol Treatment of Cognitive Dysfunction in Schizophrenia". This study is a six-week, randomized, placebo-controlled, fixed dose trial comparing cannabidiol Vs. placebo added to a stable dose of antipsychotic medications in patients diagnosed with schizophrenia.

What is the current status of trial NCT00588731?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2009-02. Estimated completion is 2013-12.

What interventions are being tested in trial NCT00588731?

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

Who is sponsoring clinical trial NCT00588731?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00588731's enrollment target sits among peer trials

41 1352nd of 2000 higher than 639 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

  • NCT03449238 · 41 participants · Phase 1

    Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients

  • NCT03900793 · 41 participants · Phase 1

    Losartan + Sunitinib in Treatment of Osteosarcoma

  • NCT04082520 · 41 participants · Phase 2

    Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy

  • NCT04220190 · 41 participants · Phase 2

    RAPA-501 Therapy for ALS

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 NCT00588731, the US trial registry maintained by the National Library of Medicine. NCT00588731 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.