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Effect of Different Timing of Endoscope Insertion on Hypoxemia and Postoperative Recovery in Patients Undergoing Propofol-Facilitated Painless Gastrointestinal Endoscopy

Effect of Different Timing of Endoscope Insertion on Hypoxemia and Postoperative Recovery in Patients Undergoing Propofol-Facilitated Painless Gastrointestinal Endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121947
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-04-07
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Patients undergoing gastrointestinal endoscopy

Interventions

QQ:Endoscope insertion 30 s–2 min after drug administration
HQ:Endoscope insertion 2-4 min after completion of drug administration

Sponsors

Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing painless gastrointestinal endoscopy 2. ASA physical status class I–III 3. New York Heart Association (NYHA) functional class I–II 4. Aged 18 to 70 years

Exclusion criteria

Exclusion criteria: 1. Patients with hypersensitivity to propofol 2. Patients with disturbance of consciousness, poor expression ability, or inability to cooperate 3. Uncontrolled life-threatening circulatory or respiratory diseases, including: Acute coronary syndrome, Severe hypertension (SBP >= 180 mmHg or DBP >= 110 mmHg), Severe arrhythmia, Heart failure, Pericardial effusion, Acute respiratory tract infection, Pulmonary edema, Pleural effusion, Asthma in acute attack, Active massive hemoptysis 4. SpO2 32 kg/m^2) 6. Acute upper gastrointestinal bleeding 7. Gastrointestinal obstruction with gastric content retention 8. Severe anemia (Hb < 60 g/L) 9. Hepatic dysfunction (Child-Pugh class C or worse) 10. Patients in whom the procedure was terminated due to unexpected events during examination

Design outcomes

Primary

MeasureTime frame
the incidence of hypoxemia;

Secondary

MeasureTime frame
the incidence of choking and cough;VAS fatigue score;recovery time;discharge time;

Countries

China

Contacts

Public ContactHongqian Huang

Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai).

hocane@163.com+86 183 8995 9630

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026