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NOT YET RECRUITING
NCT07386080
PHASE4

Carbergoline for Antipsychotic Induced Hyperprolactinemia.

Sponsor: Zealand University Hospital

View on ClinicalTrials.gov

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.

Official title: The Safety of Carbergoline Versus Placebo for Antipsychotic Induced Hyperprolactinemia: A Pragmatic, Randomised, Non-inferiority Trial With Blinded Outcome.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

146

Start Date

2026-05-01

Completion Date

2029-05-01

Last Updated

2026-02-04

Healthy Volunteers

No

Conditions

Interventions

DRUG

Cabergoline (Dopamine Agonist)

This intervention will use cabergoline for antipsychotic induced hyperprolactinemia.

DRUG

Placebo

Placebo + standard care

Locations (1)

Zealand University Hospital

Køge, Region Sjælland, Denmark