Clinical Trial

Carbergoline for Antipsychotic Induced Hyperprolactinemia.

Not Yet Recruiting Phase 4
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Summary
The goal of this clinical trial is to learn if cabergoline is safe to use in patients with antipsychotic-induced hyperprolactinemia in adults with scizophrenia. The main question it aims to answer : Is the severity of positive and negative symptoms affected by the use of cabergoline? Researchers will compare cabergolin to placebo to see if positive and negative symptoms are equel in both groups. Participants will, in a blinded manor, take either placebo tablets or cabergoline for 12 weeks. The severity of positive and negative symptoms will be evaluated before and after the intervention in both groups.
Trial Details
NCT Number NCT07386080
Lead Sponsor Zealand University Hospital
Collaborators: Region Zealand
Conditions Scizophrenia
Enrollment 146 participants
Start Date 2026-05-01
Primary Completion 2028-05-01 (estimated)
Study Completion 2029-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-04