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Clinical Trials in China / NCT04956601
Starting soon Not applicable

Adjuvant Radiotherapy in Patients With Early Endometrial Cancer

NCT04956601 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Third Hospital
Phase
Not applicable
Started
2021-07
Last updated
2021-07-09

Condition(s) studied

Endometrial CancerPathologyRadiotherapy

Investigational drug(s) / intervention(s)

vaginal brachytherapy/pelvic external beam radiotherapy

vaginal brachytherapy/pelvic external beam radiotherapy: high-dose-rate vaginal brachytherapy; pelvic external beam radiotherapy

Study summary

To compare the effect of vaginal brachytherapy as adjuvant treatment after operation when compared to pelvic external beam radiotherapy in patients with early endometrial cancer based on moderate risk molecules classification.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Endometrial adenocarcinoma is confirmed by pathology, and the molecular types were microsatellite instability type and low copy type; 2. Stage IA and grade 3 or stage IB (FIGO 2009), without substantial lymph-vascular space invasion; 3. Surgery must have included a hysterectomy and bilateral adnexectomy. Pelvic lymph node sampling and para-aortic lymph node sampling are optional; 4. ECOG score is 0-2; 5. The interval time between surgery and radiotherapy is no more than 8 weeks; 6. The routine blood examination was normal; 7. Compliance is good and informed consent is voluntarily signed. Exclusion Criteria: 1. The patients receive chemotherapy; 2. History of previous malignant disease; 3. Previous diagnosis of Crohn's disease or ulcerative colitis.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University 3rd Hospital Beijing Beijng

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04956601 on ClinicalTrials.gov ↗ ← All trials in China