BENITIONSClinical Trial Intelligence

Prophylactic Risedronate for Patients With Peripheral Lung Tumors Treated With SBRT

2상 완료 NCT03861091

대상 질환Lung Neoplasm
임상 단계2상
스폰서Wake Forest University Health Sciences
상태완료
참여자 수84 명
중재(약물)risedronate, Matching placebo
시작일2019년 7월 12일
완료일2022년 3월 2일
결과 공개일2023년 7월 14일

요약

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

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