The effect of etomidate combined with propofol applied to gastrointestinal endoscopy on postoperative fatigue syndrome

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300072610

Enrollment

Unknown

Registered

2023-06-19

Start date

2023-07-01

Completion date

Unknown

Last updated

2023-06-26

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

Conditions

Postoperative fatigue syndrome

Interventions

propofol+etomidate group:etomidate

propofol group:propofol

Eligibility

Sex/Gender

All

Age

20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with elective outpatient gastroenteroscopy 2. ASA classification: grade I-III; age: 65-85 years; BMI <25kg/m2.

Exclusion criteria

Exclusion criteria: (1) Contraindicated to anesthesia or surgery (2) Those with relevant drug allergies. (3) Patients who refuse to cooperate. (4) Patients with severe cardiopulmonary disease or cranio-cerebral injury and mental illness. (5) Patients with uncontrolled hypertension.

Design outcomes

Primary

Measure	Time frame
Incidence of postoperative fatigue syndrome;	—

Secondary

Measure	Time frame
The amount of intraoperative anesthetic drugs;	—

Countries

China

Contacts

Public ContactLi Xin

Wuxi 9th People’s Hospital Affiliated to Soochow University

55699359@qq.com+86 137 7118 9909

Outcome results

None listed

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