drugset / Trial / NCT07386080

Carbergoline for Antipsychotic Induced Hyperprolactinemia.

NCT07386080

Phase 4 Not yet recruiting 146 enrolled Zealand University Hospital Region Zealand · collab
RandomizedParallel-groupTriple-blindTreatment

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.

Timeline

Start
2026-05-01
Primary completion
2028-05-01
Completion
2029-05-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cabergoline Small molecule

Indications