drugset / Trial / NCT05487755

Investigational and Comparative Study in the Management of Diabetic Nephropathy

NCT05487755

Phase 3 Completed 90 enrolled Tanta University
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to investigate and compare the safety and efficacy of selective (PDE5) enzyme inhibitor; tadalafil and non selective (PDE) inhibitor; pentoxifylline in diabetic nephropathy to improve glucose metabolism, lipid profile and decrease albuminuria.

Timeline

Start
2022-02-01
Primary completion
2023-03-01
Completion
2023-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pentoxifylline Small molecule 400 mg Oral
Subject Tadalafil Small molecule 20 mg Oral