Hyaluronic Acid-based Gel Spacers in Gynecologic Malignancies
Recruiting
Phase 1
Interventional Study
Cervix Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Trial phase
- Phase 1
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 14 (estimated)
- Sponsor
- UNC Lineberger Comprehensive Cancer Center · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Written informed consent obtained to participate in the study and HIPAA authorization for release of personal health information.
* Subject is willing and able to comply with study procedures based on the judgment of the investigator.
* Age ≥ 18 years at time of consent.
* Eas…
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