Clinical trial
SGLT2 Inhibitor Therapy in Cystic Fibrosis-related Diabetes
Active, not recruiting · Phase 2, Phase 3 · 1 countries · Registry ID NCT06149793
What this study is about
This will be a placebo-controlled, randomized, double blind, crossover study with a 4 week wash out period. Collect pilot data on the safety, tolerability, and feasibility of empagliflozin therapy in overweight/obese patients with CFRD to support a future larger randomized controlled trial.
Basic eligibility
Full registry criteria
Treatments and study arms
Empagliflozin
Sodium glucose co-transporter 2 inhibitor
Placebo Control
Placebo Control
Primary outcomes
The primary outcomes are related to feasibility, including safety and treatment tolerability. Safety will be evaluated as the proportion (in %) of participants who experience a serious adverse event during the study. Tolerability will be evaluated as the proportion (in %) of participants who discontinue their assigned treatment due to side effects.
Study locations
1 locations were listed when this page was built. The first 40 are shown.