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A prospective randomized controlled clinical study on enhanced recover after surgery in the treatment of acute abdomen

A prospective randomized controlled clinical study on enhanced recover after surgery in the treatment of acute abdomen

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081069
Enrollment
Unknown
Registered
2024-02-21
Start date
2019-01-31
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

acute appendicitis

Interventions

Experimental group:Enhanced recovery after surgery
Control group:Traditional treatment

Sponsors

Beijing Chaoyang Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age range from 18 to 70 years old; (2) ASA score I-II; (3) Non pregnancy appendicitis; (4) No history of abdominal surgery.

Exclusion criteria

Exclusion criteria: (1) Heart and lung function cannot tolerate laparoscopic surgery; (2) formation of abscess around the appendix; (3) Individuals with abnormal coagulation function

Design outcomes

Primary

MeasureTime frame
Postoperative exhaust time;—

Secondary

MeasureTime frame
Degree of pain sensation;Postoperative hospitalization time;Hospitalization expenses;—

Countries

China

Contacts

Public ContactWang Zhenjun

Beijing Chaoyang Hospital Affiliated to Capital Medical University

drzhenjun@163.com+86 10 8523 1604

Outcome results

None listed

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