Effect of enhanced recovery after surgery clinical path on perioperative patients' short-term and long-term clinical outcomes

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000033639

Enrollment

Unknown

Registered

2020-06-07

Start date

2020-06-08

Completion date

Unknown

Last updated

2020-06-08

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

Conditions

enhanced recovery after surgery

Interventions

enhanced recovery after surgery group:Perioperative period optimize processing

Control group:Perioperative period routine processing

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. ASAI-III patients with elective surgery in Urology, Orthopedics, General Surgery, Hepatobiliary

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled cardiovascular and cerebrovascular disease, severe liver and kidney dysfunction, and bleeding disorders; 2. Patients undergoing major surgery within 1 month; 3. Those with major organ failure, mental or consciousness disorders; 4. Within 30 days before the start of the study or are participating in other clinical studies.

Design outcomes

Primary

Measure	Time frame
Length of hospitalization;Hospital costs;Pain score;Opioid dosage;The first oral intake time;Patient satisfaction;	—

Secondary

Measure	Time frame
Sleep score;Drainage tube extraction time;First exhaust time;Time to get out of bed for the first time;Complication rate during hospitalization;Complication rate six months after operation;	—

Countries

China

Contacts

Public ContactYanlin Bi

Department of Anesthesiology, Eastern Compus of Qingdao City Hospital

yanlinbi68@sina.cn+86 18661675610

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026