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Effect of Zoledronic Acid on Chemotherapy Induced Bone Loss in Non-Hodgkin's Lymphoma Patients Receiving Chemotherapy

ClinicalTrials.gov · COMPLETED, 2011

135 participants

Abstract

Primary Objective:

* Evaluate the effect of zoledronate on change in bone mineral density (BMD) at the total lumbar spine and femoral neck.

Secondary Objectives:

* Evaluate the effect of zoledronate on change in BMD at the total hip

* Evaluate risk factors for developing osteoporosis on chemotherapy

* Determine correlative markers for response to zoledronate 4. Evaluate zoledronate effect on new bone fractures 5. Evaluate the cost-effectiveness of zoledronic acid (with calcium and vitamin D) versus standard treatment (calcium and vitamin D alone).

Conditions: Non-Hodgkin's Lymphoma, Lymphoma.

Primary outcome: Percentage Change in Bone Mineral Density (BMD) T-Score From Baseline to 12 Months.

Enrollment: 135 participants.

How strong is the evidence?

Evidence Hub reads this as a clinical trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 135 participants or records.

How the five levels of evidence work. The level is assigned automatically from the abstract and can be wrong, so check the paper.

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