Clinical observation of euphoria induced by propofol

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100046127

Enrollment

Unknown

Registered

2021-05-04

Start date

2021-04-29

Completion date

Unknown

Last updated

2021-12-21

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

Conditions

Euphoria

Interventions

Case series:None

high propofol euphoria group vs. low propofol euphoria group:Nil

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Peking University Third Hospital admitted patients older than 18 years of age who planned to undergo painless gastroenteroscopy under general anesthesia.

Exclusion criteria

Exclusion criteria: 1.Refusal to sign informed consent; 2.Previous cognitive impairment, any history of neuropsychiatric diseases (such as depression), any history of drug abuse; 3.Previous allergy to propofol or adverse reactions such as propofol intolerance; 4.Language disorders, confusion, drowsiness, coma, etc. could not be evaluated preoperatively.

Design outcomes

Primary

Measure	Time frame
Euphoria;	—

Countries

China

Contacts

Public ContactXu Mao

Peking University Third Hospital

anae@163.com+86 18111482830

Outcome results

None listed

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