ERAS and Postoperative Recovery in Gynecologic Patients: A QoR-15 Study

ConditionsGynecologicERAS
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-80
SponsorNational Taiwan University Hospital

About this trial

The Quality of Recovery-15 (QoR-15) questionnaire is a widely used Patient-Reported Outcome Measure (PROM) for evaluating postoperative recovery, including pain, physical function, and emotional well-being. Enhanced Recovery After Surgery (ERAS) is a multidisciplinary care model designed to optimize perioperative management through standardized protocols.

For gynecological surgery, ERAS emphasizes preoperative education, early interventions (e.g., smoking cessation, anemia management, nutrition optimization), intraoperative strategies (e.g., fluid balance, nausea prevention, temperature control), and postoperative care (e.g., early mobilization, pain control, ileus prevention). However, while ERAS is gaining acceptance, its effectiveness can vary due to workload, patient variability, and institutional resources, and its superiority over traditional care remains inconclusive.

This study aims to objectively compare ERAS and traditional perioperative care using the QoR-15 questionnaire to assess patient satisfaction, recovery speed, surgical risk reduction, and complication prevention. Rather than solely promoting ERAS, this research seeks to evaluate its applicability, enhance personalized care, and provide scientific evidence for perioperative management optimization.

Eligibility criteria

Qualifiers

Age between 20 and 80 years.

Undergoing routine gynecological surgery, including total or subtotal hysterectomy, myomectomy, oophorectomy, gynecologic cancer staging surgery, cytoreductive surgery, and pelvic exenteration.

Cancer patients with an Eastern Cooperative Oncology Group (ECOG) performance status of ≤2.

Receiving either standard perioperative care or ERAS protocol-based care.

Disqualifiers

Age below 20 years.

Lack of decision-making capacity.

Undergoing emergency surgery.

History of clinical depression.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

130 Participants
are grouped into 2 trial groups

Locations

This trial has no locations

Sponsors and collaborators

National Taiwan University Hospital

Lead sponsor

National Taiwan University Hospital Hsin-Chu Branch

Collaborator