Enhanced Recovery After Surgery for Gynecologic Procedures

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, non-randomized study at National Taiwan University Hospital Hsin-Chu Branch compares perioperative care using an institutional ERAS protocol to conventional care in women undergoing gynecologic surgery. Participants are either enrolled in ERAS or receive standard perioperative management, and outcomes such as recovery speed, complication rates, and pain are tracked. The goal is to see if implementing ERAS improves postoperative recovery and clinical outcomes. The study collects data on perioperative factors, recovery benchmarks, and postoperative complications to evaluate the impact of ERAS in this surgical population.

Why it matters

Who can join: the full rules

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.

Where it's running

• National Taiwan University Hospital Hsin-Chu Branch
  Hsinchu, Taiwan Recruiting

Study contacts

• Principal investigator: Chia-Yi Lee, MD — National Taiwan University Hospital Hsin-Chu Branch
• Study coordinator: Chia-Yi Lee, MD
• Email: plzfixthecar@gmail.com
• Phone: +886-972652431

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.