Clinical Trials Directory

Trials / Completed

CompletedNCT03006952

Add-on Pentoxifylline to Losartan Versus Increasing Dose of Losartan on NT-PRO BNP in Type 2 Diabetics With Nephropathy

Comparative Effects of add-on Pentoxifylline to Losartan Versus Increasing Dose of Losartan on Serum NT-PRO BNP and Proteinuria in Type 2 Diabetics With Nephropathy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
59 (actual)
Sponsor
Tehran University of Medical Sciences · Academic / Other
Sex
All
Age
38 Years – 76 Years
Healthy volunteers
Not accepted

Summary

This study was designed to assess the efficacy of adding pentoxifylline to losartan in comparison with increasing dose of losartan in type 2 diabetes patients with nephropathy. also the effect of pentoxifylline on N terminal brain natriuretic peptide (NT-pro BNP) and C-reactive protein

Detailed description

Addition of pentoxifylline to losartan provides antiproteinuric effects in type 2 diabetes patients with nephropathy that might relate to its effect on N terminal brain natriuretic peptide (NT-pro BNP) and C-reactive protein. Pentoxifylline is a phosphodiestrase inhibitor with anti-inflammatory effects that was used in type 2 diabetes patients with nephropathy for treatment of diabetes complications. NT-Pro BNP, which is released from the heart due to wall stress and pressures, is known as a diagnostic and prognostic marker for heart failure and cardiovascular mortality in type 2 diabetes.

Conditions

Interventions

TypeNameDescription
DRUGPentoxifyllinepentoxifylline arm took 400 mg pentoxifylline twice daily plus 50mg losartan daily for 12 weeks.
DRUGLosartanlosartan arm took 100mg losartan daily for 12 weeks.

Timeline

Start date
2015-04-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2016-12-30
Last updated
2016-12-30

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT03006952. Inclusion in this directory is not an endorsement.