An observational study of the effect of painless gastroscopy on postoperative facial emotional recognition and interphase decision-making

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300073132

Enrollment

Unknown

Registered

2023-07-03

Start date

2023-07-28

Completion date

Unknown

Last updated

2023-07-10

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

Conditions

Cognitive impairment and addiction

Interventions

none:none

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Adult patients with American Society of Anesthesiologists Classification grades 1-2 for gastrointestinal endoscopy under general anesthesia in our hospital; 18~65 years old; BMI18.5-24 kg/m²

Exclusion criteria

Exclusion criteria: ( a ) Refusal to sign informed consent form ( b )a known hypersensitivity reaction to any drugs , such as allergy to propofol or benzodiazepines , or intolerance to them ; ( c) a history of cognitive impairment or any neuropsychiatric diseases such as depression, anxiety, Sleep disorder, etc. ( d) language disorders, blurred consciousness, drowsiness, coma, etc ( e) Nicotine, Alcohol dependence and drug addicts ( d )Drinking tea, alcohol, and stimulants in the short term ( f) a recent surgery or major trauma within 14 days prior to the experiment

Design outcomes

Primary

Measure	Time frame
facial expression recognition; interphase decision-making;	—

Secondary

Measure	Time frame
Morphine -Benzedrine Group score ;Data on intraoperative drug dosage of patients;	—

Countries

China

Contacts

Public ContactQiong Lan

Peking University Third Hospital

13810146245@163.com+86 138 1014 6245

Outcome results

None listed

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