Effect of Different Bed Head Angles on Intraoperative Hypoxemia in Patients Undergoing Painless Gastroenteroscopy: A Prospective Randomized Controlled Study

ConditionHypoxemia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorXiangya Hospital of Central South University

About this trial

Abstract:

Objective: This study aimed to investigate the effect of different bed angles (0° vs. 15°) on the incidence of intraoperative hypoxemia in patients undergoing gastroscopy and colonoscopy. A prospective randomized controlled trial was conducted to evaluate the impact of patient positioning on respiratory safety, providing evidence for individualized anesthesia management.

Background:

With the increasing popularity of painless gastrointestinal endoscopy, hypoxemia has become a major safety concern in anesthesia management, particularly in elderly and obese patients. Studies have shown that the incidence of hypoxemia can exceed 26%, highlighting the importance of optimizing respiratory safety during anesthesia.

Methods:

A total of 400 patients scheduled for painless gastrointestinal endoscopy were recruited and randomly assigned to a control group (0° left lateral position) or an experimental group (15° left lateral position). Baseline data were recorded preoperatively. Intraoperative vital signs were monitored, and the occurrence of hypoxemia and other complications was documented. Data were collected and processed in a blinded manner, followed by statistical analysis using SPSS 26.0.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Planned to undergo painless (sedated) gastrointestinal endoscopy

Signed informed consent form

American Society of Anesthesiologists (ASA) Physical Status classification I to III

Disqualifiers

Pregnancy

Emergency examination or inadequate bowel preparation

Baseline peripheral oxygen saturation (SpO₂) < 95%

Patient or family members refuse to participate in the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Elevating the head of the bed to 15 degrees

    Other intervention

    Elevating the head of the bed to 15 degrees

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Group 15°Other 1 intervention
Group B: Group 0°No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Hypoxemia

Hypoxemia (75% \< SpO₂ \< 90% lasting \> 10 seconds and \< 60 seconds)

Time frame
During the procedure

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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