BENITIONSClinical Trial Intelligence

Prophylactic Risedronate for Patients With Peripheral Lung Tumors Treated With SBRT

Phase 2 Completed NCT03861091

ConditionLung Neoplasm
PhasePhase 2
SponsorWake Forest University Health Sciences
StatusCompleted
Enrollment84 participants
Interventionsrisedronate, Matching placebo
Start dateJul 12, 2019
Completion dateMar 2, 2022
Results postedJul 14, 2023

Summary

This is a double blind randomized controlled study investigating the efficacy of a single dose of 150 mg risedronate (a bone anti-resorptive) vs a single dose of placebo given prior to SBRT for peripheral lung tumors that are within 2 cm of the chest wall. Our hypothesis is that the use of a single dose of 150 mg risedronate will eliminate or greatly reduce the rapid bone loss that occurs with radiation induced early osteoclast recruitment/activation. Patients will be given either a single dose of 150 mg risedronate or placebo at the time of their treatment mapping "simulation" CT scan. Typically, radiation treatments begin at 1 - 3 weeks following this mapping scan, as each treatment plan requires detailed physics calculations and quality assurance checks. All CT imaging referenced below is performed as a routine standard of care surveillance and is necessary for cancer treatment follow-up. These chest CT scans that are utilized in this research protocol would be performed every 3 months regardless of inclusion on this trial.

Changes in Mean Cortical Thickness

At baseline and at 3 months post radiation · percent change in mm cortical thickne

Risedronate4.24 ± 3.04 percent change in mm cortical thickne
Matching Placebo7.14 ± 2.93 percent change in mm cortical thickne

Open in BENITIONS View on ClinicalTrials.gov

Other trials for this condition

All trials

This page summarises publicly available data from ClinicalTrials.gov. It is not medical advice and not investment advice. Always consult a qualified healthcare professional.