drugset / Trial / NCT00535925

Nephropathy In Type 2 Diabetes and Cardio-renal Events

NCT00535925 ↗

Phase 4 Completed 850 enrolled University of Campania Luigi Vanvitelli
RandomizedParallel-groupOpen-labelPrevention

Summary

The NID-2 study, a multicentric study (21 centres enrolled), was planned in two phases: Phase 1(observational study, completed in September 2005): after the identification of a type-2 diabetic population with typical Diabetic Nephropathy (DN), to study of the rate of renal and cardiovascular events during a middle term follow-up. Phase 2(interventional study, started in October 2005): after randomization in two groups, a group (intervention group) is treated with an intensive multifactorial intervention whose aim is to reduce morbidity and mortality due to diabetic complications. The other group (control group) continues the conventional therapy . To avoid bias in the treatment in each center, the randomization was performed for centre.

Timeline

Start
2005-10
Primary completion
2011-12
Completion
2019-05

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper The adjusted Cox shared-frailty model demonstrated 53% lower risk of MACEs in MT arm (adjusted HR 0.47, 95%CI 0.30-0.74, P = 0.001). PMID 34271948 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlodipine Other / unclassified 10 mg —
Subject Aspirin Small molecule 160 mg —
Subject Atenolol Other / unclassified 100 mg —
Subject Clonidine Other / unclassified — —
Subject Doxazosin Unknown 4 mg —
Subject Furosemide Other / unclassified 25 mg —
Subject Furosemide Other / unclassified 75 mg —
Subject Hydrochlorothiazide Unknown 12.5 mg —
Subject Hydrochlorothiazide Unknown 25 mg —
Subject Insulin Protein / enzyme biologic — —
Subject Irbesartan Small molecule 300 mg —
Subject Ramipril Small molecule 10 mg —
Subject Simvastatin Small molecule 80 mg —
Subject epoetin alfa Protein / enzyme biologic — —