Clinical trial · Interventional
Weight Management Plus Megestrol Acetate in Early-stage Endometrioid Carcinoma
Weight Management Plus Megestrol Acetate in Early-stage Endometrioid Carcinoma: Two Single-arm, Prospective and Open-label Clinical Study
NCT05316467CI-TRIAL-00113555terminatedPhase 2 / Phase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): no enough enrolled patients
Summary
Brief summary (as posted)
To investigate the efficacy of weight management plus megestrol acetate in obese patients with early endometrioid carcinoma(EEC)asking for fertility-sparing treatment
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Endometrial Carcinoma | Endometrial Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Fertility Issues | — | UNRESOLVED | — |
| Obese | — | UNRESOLVED | — |
| Overweight | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Intensive Lifestyle Intervention (ILI) | Behavioral | — | UNRESOLVED |
| Megestrol Acetate 160 MG Oral Tablet | Drug | Megestrol | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- overweight 24kg/m2≤BMI<28kg/m2
- description
- MA+ weight management enrolled patients will receive megestrol acetate 160mg po qd plus weight management
- interventionNames
- Behavioral: Intensive Lifestyle Intervention (ILI)
- Drug: Megestrol Acetate 160 MG Oral Tablet
- type
- EXPERIMENTAL
- label
- BMI≥28kg/m2
- description
- MA+ weight management enrolled patients will receive megestrol acetate 160mg po qd plus weight management
- interventionNames
- Behavioral: Intensive Lifestyle Intervention (ILI)
- Drug: Megestrol Acetate 160 MG Oral Tablet
Primary outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 45 Years
Show eligibility criteria text
Inclusion Criteria: 1. 18 years≤age≤45years 2. BMI (body mass index) ≥24kg/m2 3. Consent informed and signed 4. Pathologically confirmed as endometrial carcinoma Patients with endometrial specimens obtained by endometrial biopsy, diagnostic curettage or hysteroscopy and diagnosed histologically as endometrioid carcinoma, G1. If specimens are from other hospitals, they must be counseled or reconfirmed by the Department of Pathology of the Obstetrics and Gynecology Hospital of Fudan University. 5. Imaging Assessment Enhanced MRI of the pelvis and enhanced CT of the upper abdomen must be performed in 2 weeks prior to starting treatment to assess the lesions confined to the endometrial layer without clear myometrial infiltration or extrauterine involvement. 6. Have a strong desire to reproduce and ask for fertility preservation or those who insist on keeping the uterus despite no reproductive requirements. 7. Have good compliance and follow-up conditions, and patients are willing to follow up in Obstetrics and Gynecology Hospital of Fudan University in time. Exclusion Criteria: 1. Patients with non-endometrioid endometrial carcinoma, endometrioid endometrial carcinoma G2/G3 or other malignant tumors of the reproductive system; imaging suggests myometrial invasion, cervical involvement or extra-uterine involvement. 2. Combined with severe medical disease or liver or kidney dysfunction: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels elevate to 3 times or more of the upper limit of normal, kidney dysfunction (creatinine clearance \<30 mL/min) 3. Patients with other types of endometrial cancer or other malignant tumors of the reproductive system; patients with breast cancer or other hormone-dependent tumors that cannot be used with progesterone. 4. Those who have received high doses of high potency progestin or oral contraceptives within the last 3 months (or those on maintenance medication). 5. Those who require hysterectomy or other methods other than conservative treatment. 6. Known or suspected pregnancy. 7. Those who has contraindications to use progestin. 8. Deep vein thrombosis, stroke, myocardial infarction. 9. Severe joint lesions that prevent walking or movement.
References
Publications (0)
Data not yet available
No reference posted for this study.