Bromocriptine for Patients With Schizophrenia and Prediabetes

PHASE4Not yet recruitingINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

January 1, 2026

Primary Completion Date

July 31, 2026

Study Completion Date

July 31, 2026

Conditions
SchizophreniaPreDiabetes
Interventions
DRUG

Bromocriptine

This is an open-label study, so there is no comparator group. As such there is only one arm. Subjects will receive bromocriptine at a starting dose of 2.5mg daily which will be increased, if tolerated, to 5mg daily after one week. Bromocriptine will be continued for a total of 6 weeks. Laboratory investigations, telephonic interviews, and face to face visits with subjects will be conducted before, during, and after the time period that bromocriptine will be used as detailed in the study design section.

Trial Locations (1)

15240

VA Pittsburgh Healthcare System, Pittsburgh

All Listed Sponsors
lead

VA Pittsburgh Healthcare System

FED