drugset / Trial / NCT02178306

Efficacy and Safety of Telmisartan in Hypertensive Patients With Mild/Moderate or Severe Renal Impairment or Requiring Hemodialysis

NCT02178306

Phase 4 Completed 82 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and efficacy, in particular with regard to renal function of telmisartan at the doses of 40 mg and 80 mg in hypertensive patients with moderate to endstage renal impairment after 12 weeks of treatment

Timeline

Start
2000-09
Primary completion
2002-04
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Telmisartan Other / unclassified 40 mg Oral
Subject Telmisartan Other / unclassified 80 mg Oral

Indications