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

NCT00288366 · ClinicalTrials.gov registry record · NA

Anticonvulsant Mood Stabilizers, Antipsychotic Drugs and the Insulin Resistance Syndrome

A NA study, sponsored by Northwestern University.

Completed
Registry status
NA
Development phase
49
Enrollment target

NCT00288366: Completed NA study, sponsored by Northwestern University.

NCT00288366 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 49 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.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00288366, a NA study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
NA
Development phase
49 participants
Enrollment target

Study Summary

The objective of this study is to determine the effect of various mood stabilizers (MS) on the insulin resistance syndrome (IRS; also called the metabolic syndrome) alone and in patients treated with antipsychotic drugs (APDs). Patients will be switched from their current antipsychotic medication to aripiprazole (Abilify) or ziprasidone (Geodon) (unless clinically contraindicated) for comparison with metabolic levels during treatment with the former medication. The metabolic syndrome is an empirical concept based on extensive evidence that a constellation of 5 metabolic abnormalities, e.g. increased cholesterol, hypertension, low HDL, taken together, predict marked increases in the risk of CVD, stroke and some types of cancer.

Primary Outcome

change in HDL ratio after medication switch

Interventions

  • DRUG ziprasidone vs. aripiprazole
  • DRUG aripiprazole vs. ziprasidone

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2006-01
Est. Completion 2008-12
Phase NA
Northwestern University

1,209 total trials

What the finished NCT00288366 record still lists

NCT00288366 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 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 2 interventions - of which ziprasidone vs. aripiprazole is the first listed.

NCT00288366 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00288366 about?

NCT00288366 is a clinical study titled "Anticonvulsant Mood Stabilizers, Antipsychotic Drugs and the Insulin Resistance Syndrome". The objective of this study is to determine the effect of various mood stabilizers (MS) on the insulin resistance syndrome (IRS; also called the metabolic syndrome) alone and in patients treated with antipsychotic drugs (APDs). Patients will be switched from their current antipsychotic medication to...

What is the current status of trial NCT00288366?

This trial is currently completed. It is a NA study. The enrollment target is 49 participants. The study started on 2006-01. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00288366?

The interventions under investigation include: ziprasidone vs. aripiprazole (DRUG), aripiprazole vs. ziprasidone (DRUG).

Who is sponsoring clinical trial NCT00288366?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00288366's enrollment target sits among peer trials

49 1379th of 2000 higher than 620 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

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

  • NCT02704858 · 49 participants · Phase 1

    Safety and Efficacy Study in Recurrent or Progressive Grade III or IV IDH1 Mutated Glioma

  • NCT03516708 · 49 participants · Phase 1

    Epacadostat (INCB024360) Added to Preoperative Chemoradiation in Patients With Locally Advanced Rectal Cancer

  • NCT03692429 · 49 participants · Phase 1

    alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells

  • NCT04329494 · 49 participants · Phase 1

    PIPAC for the Treatment of Peritoneal Carcinomatosis in Patients With Ovarian, Uterine, Appendiceal, Colorectal, or Gastric Cancer

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 NCT00288366, the US trial registry maintained by the National Library of Medicine. NCT00288366 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.