The effect of propofol on early sleep quality after gastrointestinal endoscopy was evaluated by PSQI scale

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000029032

Enrollment

Unknown

Registered

2020-01-11

Start date

2020-04-01

Completion date

Unknown

Last updated

2020-03-30

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

Conditions

Sleep

Interventions

Regular group:None

Anesthesia group:Propofol anesthesia

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who want to receive digestive endoscopy at the selected time; 2. ASA grades I ~ III; 3. Aged 18 to 65 years; 4. body mass index (BMI) 15 to 30kg/m2; 5. Non-hospital patients.

Exclusion criteria

Exclusion criteria: 1. A family history of mental illness or mental illness; 2. Severe mental or cognitive impairment; 3. Receive anesthesia again within 1 week after the examination (excluding the day of surgery); 4. Unable to cooperate with the patients (hearing and speaking disorders); 5. Heavy alcoholics or taking sedatives and sleeping pills; 6. Those with known memory or sleep dysfunction; 7. Inpatient after examination; 8. Suspected or confirmed gastrointestinal malignancy; 9. Contraindications of digestive endoscopy; 10. Allergic to propofol.

Design outcomes

Primary

Measure	Time frame
Score of PSQI scale;	—

Secondary

Measure	Time frame
Satisfaction score;Lesion detection rate;	—

Countries

China

Contacts

Public ContactGaofeng Zhao

Guangdong Provincial Hospital of Traditional Chinese Medicine

zhaogaofeng-97@163.com+86 15920387021

Outcome results

None listed

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