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Carbergoline for Antipsychotic Induced Hyperprolactinemia.
Sponsor: Zealand University Hospital
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
Cabergoline (Dopamine Agonist)
This intervention will use cabergoline for antipsychotic induced hyperprolactinemia.
Placebo
Placebo + standard care
Locations (1)
Zealand University Hospital
Køge, Region Sjælland, Denmark