Monday, October 26, 2026 · Daily editionET --:--:--

Not recruiting yet

SHAPE-ENDO: Pilot Randomized Trial of Multimodal Pre-Surgical Optimization Versus Standard Surgery in Patients With Obesity and Early-Stage Endometrial Cancer

NCT07462663 · Hospital Universitari de Bellvitge · Updated 10 June 2026

What is being tested
GLP-1 Receptor Agonist; Levonorgestrel IUD (Lng-IUD); Oral Progestins; Dietetic-Nutritional intervention; Structured Exercise and Prehabilitation Program; Endometrial Biopsy With or Without Hysteroscopy; Radiologic Surveillance (MRI and Transvaginal Ultrasound); Standar upfront Surgery
For
Endometrial Cancer; Endometrial Cancer Stage I; Atypical Endometrial Hyperplasia and Endometrial Carcinoma Stage I; Atypical Endometrial Hyperplasia; Endometrial Intraepithelial Neoplasia; Obesity & Overweight; BMI>40; Obesity; Obesity Grade III
Kind of study
Tests a treatment or device on volunteers. Phase 4.
Who can join
Ages 18 years and older. About 80 people. The full rules are on the registry page.
Where
Not stated
When
Starts or started Jan 2027, ends Jan 2035. Registered 10 March 2026.
Results
None posted yet.

In the researchers' words

SHAPE-ENDO is a single-center, open-label, pilot randomized clinical trial conducted at Hospital Universitari de Bellvitge in Barcelona, Spain. The study will evaluate the feasibility, safety, and acceptability of comparing two treatment strategies in women with atypical endometrial hyperplasia/endometrial intraepithelial neoplasia or low-risk endometrioid endometrial cancer and grade III obesity, defined as BMI ≥40 kg/m². Eligible participants will be randomized in a 1:1 ratio to one of two arms. The control arm will undergo standard immediate surgery according to the institutional clinical protocol. The experimental arm will receive the SHAPE-ENDO multimodal pre-surgical optimization strategy before surgery. The SHAPE-ENDO strategy includes metabolic treatment with semaglutide/Wegovy®, local hormonal therapy with a levonorgestrel-releasing intrauterine device/Mirena® with or without oral medroxyprogesterone acetate/Progevera®, a structured nutritional program, adapted physical exercise, and scheduled oncologic surveillance with clinical evaluation, imaging, and endometrial biopsy with or without hysteroscopy. The experimental strategy will initially last 28 weeks. In participants with clinical, metabolic, or anthropometric benefit, adequate tolerance, and no evidence of tumor progression, the strategy may be extended up to 54 weeks before surgery. The primary objective…
ClinicalTrials.gov, NCT07462663