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Clinical evaluation of Ehanced Recovery After Suegery (ERAS) in gynecological laparoscopic surgery

Clinical evaluation of Ehanced Recovery After Suegery (ERAS) in gynecological laparoscopic surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045117
Enrollment
Unknown
Registered
2021-04-07
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

Benign gynecologic diseases to be treated with laparoscopic surgery

Interventions

ERAS Group:ERAS Plan
Routine Group:routine peri-operative plan

Sponsors

Shenzhen Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients went through laparoscopy in gynecology depatment from August,2019 to December,2020.

Exclusion criteria

Exclusion criteria: 1. Patients who went through emergency operation at the date of admission; 2. Patients with gynecological malignant tumor.

Design outcomes

Primary

MeasureTime frame
post op pain rate;postoperative nausea and vomiting rate;—

Secondary

MeasureTime frame
post op urinary retention rate;post op fever rate;post op VTE rate;post op abdomen distention rate;post op first urination time;post op first anal gas pass time;post op first defecation time;—

Countries

China

Contacts

Public ContactDu Xuelian

Shenzhen Traditional Chinese Medicine Hospital

jndxl@hotmail.com+86 15919778851

Outcome results

None listed

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