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NCT06326840

Clinical Efficacy and Adverse Reactions of Antipsychotic Treatment

Completed NA Last updated 22 March 2024
What this trial tests

NA trial testing Metformin in Metabolic Disturbance in 42 participants. Completed in 10 June 2011.

Timeline
31 May 2010
Primary endpoint
10 June 2011
10 June 2011

Quick facts

Lead sponsorTaipei Medical University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment42
Start date31 May 2010
Primary completion10 June 2011
Estimated completion10 June 2011
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Taipei Medical University Hospital

Who can join

Adults 18 to 60, any sex, with Metabolic Disturbance or Hyperprolactinemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to explore the potential of metformin in managing olanzapine-induced metabolic disturbance and hyperprolactinemia in patients with schizophrenia. The main questions it aims to answer are: 1. The effect of metformin on olanzapine-induced metabolic disturbance 2. The effect of metformin on olanzapine-induced hyperprolactinemia Participants will receive metformin 1500 mg/day for 8 weeks and assessments every 2 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Metformin

Trials testing the same drug.

Other recruiting trials for Metabolic Disturbance

Currently open trials in the same condition.

Other Taipei Medical University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT06326840.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing