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NOT YET RECRUITING
NCT07688070
PHASE4

Verapamil Effect in Cystic Fibrosis-related Dysglycemia

Sponsor: Rhode Island Hospital

View on ClinicalTrials.gov

Summary

We are conducting a pilot open-label pre/post interventional trial in adolescents and adults with cystic fibrosis (CF) and abnormal glucose tolerance or early CF-related diabetes mellitus (CFRD) to assess the safety and efficacy of verapamil on beta cell function and dysglycemia.

Official title: The Effect of Verapamil on Beta Cell Function in Adolescents and Adults With Cystic Fibrosis-related Dysglycemia

Key Details

Gender

All

Age Range

14 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-07-01

Completion Date

2028-08-31

Last Updated

2026-07-07

Healthy Volunteers

No

Interventions

DRUG

Verapamil Hydrochloride

Verapamil extended release (ER) will be initiated at a dose of 120mg daily and up-titrated over six weeks to target dose of 360mg daily as tolerated.

Locations (2)

Diabetes Research Center, Massachusetts General Hospital

Boston, Massachusetts, United States

Rhode Island Hospital

Providence, Rhode Island, United States