Actively Recruiting
PROton Therapy for Post Surgical Treatment of GYNecologic Cancer
Led by Abramson Cancer Center at Penn Medicine · Updated on 2026-03-12
25
Participants Needed
3
Research Sites
155 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a single institution, multi-center, Phase II, single-arm study, using Whole Pelvis (WP) Pencil Beam Scanning Proton Radiation (PBS PRT) in the post-surgical, adjuvant setting for definitive treatment of gynecologic cancers. The purpose of this study is to estimate rate of acute clinician-reported gastrointestinal (GI) toxicity using WP PBS PRT in the definitive treatment of gynecologic cancers in the post-surgical, adjuvant setting.
CONDITIONS
Official Title
PROton Therapy for Post Surgical Treatment of GYNecologic Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically confirmed cervical or endometrial cancer
- Indication for adjuvant whole pelvic radiation therapy, with or without systemic therapy
- Age of 18 years or older
- Written informed consent
- ECOG of 0-2 within 3 months of enrolling
You will not qualify if you...
- Prior course of pelvic radiation
- Metastatic disease outside of the pelvis
- Active inflammatory bowel disease
- Incapacity to provide informed consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
Virtua Health
Voorhees Township, New Jersey, United States, 08043
Actively Recruiting
2
Lancaster General Health - Ann B. Barshinger Cancer Institute
Lancaster, Pennsylvania, United States, 17601
Actively Recruiting
3
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
P
Project Manager
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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