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NCT00472641
Adjunctive Ziprasidone in Overweight and Obese Patients With Bipolar Disorder
Phase 4 trial testing Ziprasidone/Geodon in Bipolar Disorder in 25 participants. Completed in 1 December 2009.
1 December 2009
Quick facts
| Lead sponsor | Stanford University |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 25 |
| Start date | 1 January 2007 |
| Primary completion | 1 December 2009 |
| Estimated completion | 1 December 2009 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Ziprasidone/Geodon — full drug profile →
Conditions studied
- Bipolar Disorder — all drugs for Bipolar Disorder →
Sponsor
Stanford University
Who can join
Adults 18 to 65, any sex, with Bipolar Disorder. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
The Primary Outcome Measure Was Weight Change From Baseline to Endpoint.
Time frame: Baseline, 12 weeks
The primary outcome measure will be the change in weight from baseline to endpoint using a random regression mixed effects model.
Sponsor's own description
This research study is designed to determine if replacing your current antipsychotic and/or mood stabilizer with ziprasidone (Geodon) will impact weight. This research is being conducted because Geodon has a documented effect on mood. Additionally, we believe Geodon to be an effective medication for overweight or obese patients with bipolar disorder. There will be approximately 25 patients enrolled in this study.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Interventions for the management of obesity in people with bipolar disorder.
Tully A, Smyth S, Conway Y, Geddes J, et al · · 2020 · cited 18× · PMID 32687629 · DOI 10.1002/14651858.cd013006.pub2
Verify or expand the search:
- PubMed search for NCT00472641
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00472641 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Stanford University
- Last refreshed: 29 March 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00472641.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing