drugset / Trial / NCT02074631

Prevention of Bone Loss After Pediatric Hematopoietic Cell Transplantation

NCT02074631

Phase 2 Completed 63 enrolled Masonic Cancer Center, University of Minnesota
RandomizedParallel-groupOpen-labelPrevention

Summary

This is a Phase 2, open-label, randomized, controlled clinical study of pediatric subjects treated with pamidronate with calcium and vitamin D versus calcium and vitamin D alone following hematopoietic cell transplantation (HCT). The purpose of this study is to test the hypothesis that subjects receiving pamidronate with calcium and vitamin D will have higher lumbar spine bone mineral content (LBMC) measured by dual-energy X-ray tomography (DXA) at 1 year post-HCT than subjects receiving calcium and vitamin D alone (Control Group).

Timeline

Start
2015-02
Primary completion
2022-10-06
Completion
2022-10-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamidronate Small molecule 1 mg/kg
Background Calcium carbonate Other / unclassified
Background Cholecalciferol Other / unclassified 600 iu
Background Ergocalciferol Small molecule 600 iu

Indications