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Application of enhanced recovery after surgery in gynecological benign tumor operation

Application of enhanced recovery after surgery in gynecological benign tumor operation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033209
Enrollment
Unknown
Registered
2020-05-24
Start date
2020-06-23
Completion date
Unknown
Last updated
2020-05-25

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

Conditions

Gynecological benign tumor

Interventions

Experimental group:Perioperative management of ERAS
Control group:Traditional perioperative management

Sponsors

Fujian Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients with gynecological benign tumors; 2. Patients planning to undergo gynecological benign tumor surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant tumors; 2. Patients who are participating in other clinical studies; 3. Patients that researchers think it is not suitable for clinical researchers.

Design outcomes

Primary

MeasureTime frame
The length of hospital stay;pain scores;complications;rehospitalization rates;—

Countries

China

Contacts

Public ContactQibin Wu

Fujian Maternity and Child Health Hospital

fjfy_fkzl@163.com+86 591-87279671

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026