Postoperative Hypofractionated Whole Pelvic Radiotherapy in Cervical and Endometrial Cancer
Recruiting
N/A
Interventional Study
Endometrial Cancer
Cervix Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 120 (estimated)
- Sponsor
- Siriraj Hospital · Other
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About This Trial
This study aims to evaluate a shorter course of postoperative pelvic radiotherapy in patients with cervical and endometrial cancer. The standard radiotherapy schedule usually requires many treatment sessions over several weeks, which can be burdensome for patients and may affect their ability to complete treatment.
This study will compare a shorter radiotherapy schedule (hypofractionated radiothe…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Pathologically proven carcinoma of the uterine cervix; and carcinoma and carcinosarcoma of uterine corpus
2. Hysterectomy (total abdominal hysterectomy, vaginal hysterectomy, total laparoscopic hysterectomy or radical hysterectomy) for cancer of the cervix or endometrium with…
Contacts