Enhanced Recovery After Surgery (ERAS) in Patients Undergoing Gynecologic Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorNational Taiwan University Hospital
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Enhanced Recovery After Surgery (ERAS)
- Conventional Perioperative Care
Treatment groups
200 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov