drugset / Trial / NCT00376883

Pamidronate Prophylaxis in Multiple Myeloma 30 mg/Month Versus 90 mg/Month

NCT00376883

RandomizedParallel-groupDouble-blindPrevention

Summary

Multiple myeloma is a malignant hematological disease dominated by monoclonal plasma cells in the bone marrow. Major symptoms are related to the bones due to an increased bone resorption and a decreased bone formation leading to bone pain and increased risk of fractures. The normal osteoclasts are responsible for bone degradation through stimulation from the malignant plasma cells. Bisphosphonates have been shown to inhibit the osteoclast activity but may have serious side-effects due to renal toxicity and the optimal dose have not been established. In a randomized double blinded design it is aim to compare the standard of monthly injections of 90 mg pamidronate with 30 mg. The primary end-point is physical function estimated by EORTC QLQ-C30 questionnaire at 12 months after starting the treatment in newly diagnosed treatment demanding multiple myeloma. Secondary end-points are skeletal related events, cost-utility analysis, response, response duration and survival and quality of life with respect to fatigue and pain.

Timeline

Start
2000-01
Primary completion
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamidronate Small molecule 30 mg Intravenous
Subject Pamidronate Small molecule 90 mg Intravenous

Indications