drugset / Trial / NCT00738257

A Prospective, Multicentre, Open-label Randomised Controlled Study to Investigate the Effectiveness of Pamidronate in the Prevention of Bone Loss in de Novo Renal Transplant Patients.

NCT00738257

Phase 4 Completed 126 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study was to evaluate the effect of Pamidronate on bone mineral density loss and fracture rates up to 2 years, in post renal-transplant subjects on a Ciclosporin A and glucocorticoid based immunosuppressive regimen.

Timeline

Start
2000-06
Primary completion
2004-12
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamidronate Small molecule 1 mg/kg