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RECRUITING
NCT07045935
PHASE4

Metabolic Outcomes in Patients With Prolactinomas Under Dopamine Agonist Treatment

Sponsor: University Hospital, Basel, Switzerland

View on ClinicalTrials.gov

Summary

This randomized, active-controlled, parallel-arm, single-blind trial is to compare the effects of Dopamine agonists (DA) therapy targeting different established treatment strategies on glucose metabolism assessed by an oral glucose tolerance test.

Official title: Metabolic Outcomes in Patients With Prolactinomas Under Dopamine Agonist Treatment - A Randomized, Single-Blind Active- Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-09-16

Completion Date

2029-12-31

Last Updated

2025-09-23

Healthy Volunteers

No

Conditions

Interventions

DRUG

Cabergoline (Dopamine Agonist)

Cabergoline is available in tablet form, with doses of 0.5 mg per tablet. The standard dosing for hyperprolactinemia typically starts at 0.25 mg to 0.5 mg per week, which can be gradually increased based on the patient's response, with a usual range of 0.25 mg to 2 mg per week. The dose required to achieve the target prolactin levels (pre- defined for each intervention arm) may vary between patients, so a fixed dose is not specified. This allows for individualized treatment based on each patient's response.

Locations (1)

University Hospital Basel, Dept. of Endocrinology, Metabolism & Diabetes

Basel, Switzerland