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ACTIVE NOT RECRUITING
NCT04033081
PHASE4

Registry of Sarcoma Patients Treated With Permanently Implantable LDR CivaSheet®

Sponsor: CivaTech Oncology

View on ClinicalTrials.gov

Summary

This patient study will determine the safety and toxicity of a permanently implantable brachytherapy source - CivaSheet® - which is designed to deliver a therapeutic dose of low dose rate (LDR) radiation with polymer encased Palladium-103. CivaSheet will be implanted in sarcoma patients with disease presenting in the retroperitoneum, abdomen, pelvis and trunk.

Official title: Registry of Retroperitoneal, Abdominal, Pelvic and Truncal Sarcoma Patients Treated With Permanently Implantable LDR CivaSheet® to Evaluate the Safety and Feasibility Over 5 Years

Key Details

Gender

All

Age Range

Any - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2020-04-30

Completion Date

2030-04

Last Updated

2026-03-23

Healthy Volunteers

No

Conditions

Interventions

DEVICE

CivaSheet

Implanting CivaSheet radiation therapy device at the time of surgery to irradiate surgical margin potentially preventing local recurrence

Locations (1)

Fox Chase Cancer Center

Philadelphia, Pennsylvania, United States