CompletedNot Applicable

Multimodal Prehabilitation Program for Women Undergoing Gynecologic Oncology Surgery

Egypt140 participantsStarted 2024-04-23

Plain-language summary

The goal of this clinical trial is to evaluate the role of multimodal Prehabilitation program on improve surgical outcomes after gynecological oncology surgery.

Who can participate

Age range18 Years – 70 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Newly diagnosed woman with gynecologic cancer by imaging \&histopathology * Accept participation in the study. Exclusion Criteria: * Patient with advanced and metastatic stage * Patient who received neoadjuvant chemotherapy * Patient who have psychological disorder such as suicidal attempt * Patient who have cerebral stroke, hemiplegia or paralyses

What they're measuring

changing the postoperative morbidity

Timeframe: "up to 30 days postoperative"

changing the postoperative mortality

Timeframe: "up to 30 days postoperative"

Pain intensity measured by the Visual Analog Scale (VAS) for pain.

Timeframe: "up to 30 days postoperative"

Trial details

NCT IDNCT07188662

SponsorAssiut University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04-23

View on ClinicalTrials.gov More Gynecologic Oncology Patient trials