Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies
NCT: NCT07292818 · RECRUITING
Brief Summary
This pilot feasibility study evaluates the use of a hyaluronic acid-based spacing gel (Barrigel) in participants with cervical cancer undergoing chemoradiotherapy (chemoRT), including brachytherapy, as part of standard care. The primary goal is to assess feasibility. Other goals include determining whether gel placement can reduce radiation dose to nearby healthy organs (organs at risk, OAR) and improve delivery of the prescribed radiation dose to the tumor. In cervical cancer, the radiation dose to the tumor is often limited by the risk of exposing nearby sensitive organs, such as the rectum, bladder, and other pelvic structures. Vaginal packing techniques and specialized devices are used to protect these organs and ensure effective treatment. Gel spacers are inserted before radiation therapy to create space between the rectum and the cervix, reducing radiation exposure to healthy tissue. Already widely used in prostate cancer treatment in the U.S., gel spacers may also help improve tumor control and reduce treatment-related toxicity in cervical cancer.
Frequently Asked Questions
What is Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies?
Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies is a clinical trial registered under NCT07292818. Current status: RECRUITING.
What is the status of NCT07292818?
The current status of NCT07292818 (Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies) is: RECRUITING.
When did Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies start?
Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies started on 2026-02-02.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.