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NCT Number: NCT07764276

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

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.

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Key information

Conditions

ERAS Gynecologic Oncological Pelvic/Abdominal Surgery Gynecologic Surgery

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

National Taiwan University Hospital Hsin-Chu Branch

Hsinchu, Taiwan

Location status: Recruiting

Location contact

Chia-Yi Lee, MD

CONTACT

[email protected]

+886-972652431

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Enhanced Recovery After Surgery (ERAS)

Other

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

Conventional Perioperative Care

Other

Standard perioperative care according to routine institutional practice.

Primary outcomes

  1. Time to First Ambulation

    Time frame: Up to 3 days after surgery

    Time from return to the hospital ward after surgery to the first ambulation, defined as leaving the bed and standing independently.

  2. Postoperative Pain Score

    Time frame: 4, 8, 16, 24, 48 hours after surgery

    Postoperative 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 outcomes

  1. Time to First Gas Passage

    Time frame: Up to 7 days after surgery

  2. Time to First Stool Passage

    Time frame: Up to 7 days after surgery

  3. Time to removal of Foley catheter

    Time frame: Up to 7 days after surgery

  4. Postoperative nausea or vomiting

    Time frame: Up to 7 days after surgery

  5. Overall Postoperative Complication Rate

    Time frame: Up to 90 days after surgery

  6. Length of Hospital Stay

    Time frame: Up to 14 days after surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Chia-Yi Lee, MD

CONTACT

[email protected]

+886-972652431

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Aug 13, 2026
Registry last updated
Aug 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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