Pre-habilitation Within ERAS Protocol for Gynecologic Oncology Surgery: The Pre_ERAS Study

Recruiting now · Not applicable

Conditions studied: ERAS, Compliance, Quality of Life (QOL), Excercise, Immunonutrition, Post Operative Pain, Laparotomy Patients, Surgical Complication, Gynaecological Malignancies, Gynaecologic Cancer, Gynaecological Oncology

In brief

ERAS (Enhanced Recovery After Surgery) protocols are step-by-step care plans that help patients recover faster after surgery. They focus on keeping the body's normal functions, lowering stress from surgery, and supporting a quicker recovery. In gynecologic cancer surgeries, ERAS has been shown to help patients do better, have fewer problems, and leave the hospital sooner. A prehabilitation program, in combination with ERAS protocols, aims to optimize patients' physical and psychological condition prior to surgery for gynecological cancers. Interventions may include tailored exercise, nutritional support, respiratory training, and psychological preparation. By enhancing baseline fitness and resilience, prehabilitation improves the body's ability to tolerate surgical stress, reduces complications, and facilitates a faster, smoother recovery within the ERAS framework.

Key facts

Study ID

NCT07210164

Run by

Aristotle University Of Thessaloniki

People needed

100

Starts

2025-12-01

Expected to finish

2029-12-30

Last updated by the study team

2025-10-07

Who can join

Age: 18 and older, up to 85. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Type of gynecological malignancy: endometrial cancer, ovarian cancer, cervical cancer, treated with laparotomy after the decision of the gynecological-oncology unit (positive opinion of the Multidisciplinary Tumor Board - MDT)
• Patient age: 18 to 85 years
• General condition of the patient: ASA score I-III
• Consent to implement the accelerated recovery protocol - Enhanced recovery after surgery (ERAS)
• Sufficient understanding of the Greek language
• Provision of signed, after thorough information, consent to participate in the study

You may not qualify if…

• Women with performance status: ECOG >2 and ASA score >III
• Women who have not been informed and have given written consent

Where it is running

• General Hospital of Papageorgiou — Thessaloniki, Greece (enrolling)

Full record on ClinicalTrials.gov

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