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Enhanced Recovery After Surgery (ERAS) in Patients Undergoing Gynecologic Surgery

The Effect of Enhanced Recovery After Surgery (ERAS) Program in Patients Undergoing Gynecologic Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07764276
Enrollment
200
Registered
2026-08-13
Start date
2024-05-16
Completion date
2027-12-01
Last updated
2026-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ERAS, Gynecologic Surgery, Gynecologic Oncological Pelvic/Abdominal Surgery

Brief summary

Enhanced Recovery After Surgery (ERAS) is a multidisciplinary perioperative care program designed to reduce surgical stress, accelerate postoperative recovery, and improve clinical outcomes. This prospective, non-randomized study aims to evaluate the effectiveness of an ERAS program in patients undergoing gynecologic surgery at National Taiwan University Hospital Hsin-Chu Branch. Patients who choose to participate in the ERAS program will receive perioperative care according to the institutional ERAS protocol, while those who choose conventional perioperative care will serve as the comparison group. Perioperative outcomes, postoperative recovery, postoperative complications, pain scores, and other clinical outcomes will be compared between the two groups to evaluate the clinical impact of implementing an ERAS program.

Interventions

A multidisciplinary perioperative care program designed to reduce surgical stress and enhance postoperative recovery.

Standard perioperative care according to routine institutional practice.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female scheduled for laparotomic gynecologic surgery (including hysterectomy, myomectomy, adenomyomectomy, oophorectomy or oophrocystectomy, staging surgery, debulking surgery or interval debulking surgery) * 18 years old or older * American Society of Anesthesiologists Physical Status classification I to III.

Exclusion criteria

* Female undergo laparoscopic surgery but are converted to laparotomic surgery * History of delayed gastric emptying, gastrointestinal motility disorders or chronic pain * Female undergo emergent surgery.

Design outcomes

Primary

MeasureTime frameDescription
Time to First AmbulationUp to 3 days after surgeryTime from return to the hospital ward after surgery to the first ambulation, defined as leaving the bed and standing independently.
Postoperative Pain Score4, 8, 16, 24, 48 hours after surgeryPostoperative pain intensity will be assessed using the Numerical Rating Scale (NRS), ranging from 0 to 10, with 0 indicating no pain and 10 indicating the worst possible pain. Higher scores indicate greater pain intensity.

Secondary

MeasureTime frame
Time to First Gas PassageUp to 7 days after surgery
Time to First Stool PassageUp to 7 days after surgery
Time to removal of Foley catheterUp to 7 days after surgery
Postoperative nausea or vomitingUp to 7 days after surgery
Overall Postoperative Complication RateUp to 90 days after surgery
Length of Hospital StayUp to 14 days after surgery

Countries

Taiwan

Contacts

CONTACTChia-Yi Lee, MD
plzfixthecar@gmail.com+886-972652431
PRINCIPAL_INVESTIGATORChia-Yi Lee, MD

National Taiwan University Hospital Hsin-Chu Branch

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026