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Effect of Semirecumbent Position on incidence of hypoxia during sedated Left-Lateral gastrointestinal endoscopy in Elderly patients

Effect of Semirecumbent Position on incidence of hypoxia during sedated Left-Lateral gastrointestinal endoscopy in Elderly patients: Single-Center Randomized Controlled Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115036
Enrollment
Unknown
Registered
2025-12-22
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Gastrointestinal endoscopy is an important examination for the screening, diagnosis and treatment of gastrointestinal diseases.

Interventions

0° semi-recumbent position group (Group A):0° semi-recumbent position with the left lateral position
15° semi-recumbent position group (Group B):15° semi-recumbent position with the left lateral position
30° semi-recumbent position group (Group C):30° semi-recumbent position with the left lateral position

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 60 and <=90 years old; 2.Planned to sedated gastrointestinal endoscopy (including gastroscopy and/or colonoscopy); 3.American Society of Anesthesiologists (ASA) classification of grades I to III; 4.Patient or their legal representative has signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Severe cardiopulmonary dysfunction; 2. Body mass index (BMI) >=35 kg/m^2; 3. Inability to tolerate left lateral or semi-recumbent position; 4. Pre-existing hypoxemia (SpO2 <=90%); 5. Severe neurological disease affecting respiratory function; 6. Use of drugs that may impair respiratory function prior to the procedure without discontinuation; 7. Patient or their legal representative refuses to participate in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of hypoxemia;

Secondary

MeasureTime frame
The incidence of respiratory depression;The patient's satisfaction score;Adverse event;The operator's examination comfort;The incidence of severe hypoxia;

Countries

China

Contacts

Public ContactJun Dong

The First Affiliated Hospital of Chongqing Medical University

dongjun441@163.com+86 23 89011876

Outcome results

None listed

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