Actively Recruiting
Spatially Fractionated Radiation Treatment for Gynaecological Cancers
Led by Tata Memorial Hospital · Updated on 2026-02-20
20
Participants Needed
1
Research Sites
229 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective study to evaluate in-field disease control, survival and late toxicity in patients with cervical cancer or pelvic recurrence treated with spatially fractionated RT. The study will include patients with primary cervical cancer or pelvic recurrence not suitable for brachytherapy in view of anticipated or actual suboptimal target coverage due to aberrant anatomy or large residual disease at the time of brachytherapy.
CONDITIONS
Official Title
Spatially Fractionated Radiation Treatment for Gynaecological Cancers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients aged 18 to 70 years
- Cervical cancer patients post external beam radiation therapy with expected poor brachytherapy dose coverage due to aberrant pelvic anatomy or large residual disease
- Patients with very narrow vaginal canal unsuitable for intracavitary or vaginal cylinder applicators
- Inoperable endometrial cancer patients not suitable for anesthesia or with anticipated poor brachytherapy coverage
- Patients with large pelvic recurrences after surgery and/or chemotherapy or radiation not suitable for surgical salvage or brachytherapy
- Patients with contraindications to anesthesia for brachytherapy with risk of adverse events
You will not qualify if you...
- Any pre-existing fistula in bladder or rectum
- Presence of pelvic prosthesis
- Refusal to provide consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
ACTREC Tata Memorial Centre
Navi Mumbai, Maharashtra, India, 410210
Actively Recruiting
Research Team
S
Supriya Chopra, MD
CONTACT
A
Ankita Gupta, MD
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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