Study on the Promoting Effect of Optimized Perioperative Management of Gynecologic Laparoscopic Surgery on Enhanced Recovery After Surgery (ERAS): A Randomized Controlled Clinical Trial.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300079031

Enrollment

Unknown

Registered

2023-12-24

Start date

2023-12-24

Completion date

Unknown

Last updated

2024-01-08

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

Conditions

Gynecolog

Interventions

Intervention group:early removal of urinary catheter, early resumption of oral intake, and controlled fluid replacement

control group:NONE

Eligibility

Sex/Gender

Female

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Absence of contraindications for laparoscopic surgery. 2. Patients undergoing gynecologic benign surgeries who meet the indications for laparoscopic surgery. 3. Age between 18 and 70 years. 4. Preoperative hemoglobin level > 7g, surgical duration less than 6 hours, and intraoperative blood loss less than 800ml.

Exclusion criteria

Exclusion criteria: 1. Presence of contraindications for laparoscopic surgery. 2. History of other malignancies or preoperative history of radiation or chemotherapy. 3. History of more than 2 pelvic surgeries, bowel obstruction, or intraoperative intestinal procedures in the current surgery. 4. History of urinary incontinence. 5. History of mental illness.

Design outcomes

Primary

Measure	Time frame
Discharge time;	—

Secondary

Measure	Time frame
First time to get out of bed;exhaust time;	—

Countries

CHINA

Contacts

Public ContactZHANG YUE

First Maternal and Infant Health Hospital

yzhang2013@126.com+86 136 4170 4269

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026