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NCT07116213

Clinical Research on Moderately Hypofractionated Adaptive Postoperative Radiotherapy for High-Risk Endometrial Cancer

Recruiting now NA Last updated 11 August 2025
What this trial tests

NA trial testing Moderately Hypofractionated Adaptive Radiotherapy in Endometrial Cancer in 20 participants. Currently enrolling.

Timeline
30 June 2025
Primary endpoint
30 June 2029
30 December 2030

Quick facts

Lead sponsorXiaorong Hou
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date30 June 2025
Primary completion30 June 2029
Estimated completion30 December 2030
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Xiaorong Hou

Who can join

Adults 18 to 70, female only, with Endometrial Cancer or Hypofractionated Dose. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

1. Study Type: Single-center, single-arm, prospective study. 2. Sample Size: 20 patients with high-risk endometrial cancer were enrolled. 3. Treatment Procedure: The existing clinical oART (Online Adaptive Radiotherapy) workflow protocol for malignant tumors used in our department was applied. Procedures included simulation, target volume delineation, radiotherapy planning, and treatment delivery. External beam radiation therapy (EBRT) was delivered using moderate hypofractionation. If indicated, brachytherapy was performed after the completion of EBRT. When combined with chemotherapy, radiotherapy could be administered during chemotherapy intervals or after completion of chemotherapy. 4. Study Endpoints: Primary Endpoint: Incidence of acute toxicity. Secondary Endpoints: 3-year failure-free survival (FFS) rate, incidence of chronic toxicity, quality of life (QoL), treatment costs, etc.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Endometrial Cancer

Currently open trials in the same condition.

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Data sources for this page

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