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Left semi-recumbent position during painless endoscopic ultrasonography and perioperative hypoxemia: a randomized controlled clinical trial

Left semi-recumbent position during painless endoscopic ultrasonography and perioperative hypoxemia: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115230
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-12-25
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

Hypoxemia

Interventions

0° left lateral position group (L0° group):Lie on the left side with the head of the bed raised by 0°
15° left semi-recumbent position group (L15° group):Semi-reclining position on the left side, with the head of the bed elevated by 15 degrees
30° left semi-recumbent position group (L30° group):Semi-reclining position on the left side, with the head of the bed elevated by 30 degrees

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. Gender is not limited; 3. Body mass Index (BMI) : 18.5-30kg/m ²; 4.ASA is classified into grades I to III; 5. Endoscopic ultrasound examination of the upper digestive tract (esophagus, stomach); 6. Be able to understand the plan and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with difficult airways; 2. Patients with high-risk factors such as reflux and aspiration; 3. History of upper gastrointestinal surgery; 4. Previous lung surgeries, pneumothorax, pulmonary tuberculosis, and pleural effusion; 5. Have respiratory diseases (chronic obstructive pulmonary disease, respiratory tract infections, pulmonary infections, asthma, emphysema, etc.); 6. Patients with severe liver or kidney dysfunction; 7. Patients with anemia; 8. Pregnant patients; 9. History of mental illness;

Design outcomes

Primary

MeasureTime frame
The incidence of hypoxemia during the examination (SpO2 10 seconds);

Secondary

MeasureTime frame
The occurrence of body movement response (involuntary limb or body movement in patients during endoscopic ultrasound examination) during the examination;Degree of choking cough during the examination (Grade I: No choking cough, even breathing; Grade II: Single mild choking cough; Grade III: multiple choking coughs, but lasting less than 15 seconds; Grade IV: Continuous choking cough, lasting more than 15 seconds);The incidence of severe hypoxemia (SpO2 10 seconds);The lowest blood oxygen saturation during the examination and recovery period;Dosage of propofol;Duration of recovery;Respiratory comfort in the anesthesia recovery room (scored using a numerical assessment scale, with a score range from 0 to 10, and the higher the score, the more comfortable it is);The duration of stay in the anesthesia recovery room;The use of vasoactive drugs (atropine, ephedrine) during the examination period;Record HR, MAP and SpO2 before anesthesia induction (T0), when the endoscope passes through the throat (T1), at the beginning of endoscopy (T2), at the end of endoscopy (T3), when the patient wakes up (T4), and when leaving the anesthesia recovery room (T5);Record the satisfaction scores of patients (after regaining consciousness), anesthesiologists, recovery room nurses and digestive endoscopists;Record the occurrence of adverse reactions such as nausea, vomiting and laryngeal spasm in patients;

Countries

China

Contacts

Public ContactXiaoyong Wei

General Hospital of Ningxia Medical University

weixy9912@126.com+86 173 9506 1735

Outcome results

None listed

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