Effect of Different Body Positions on Hypoxemia During Recovery in Patients Undergoing Painless Gastroscopy and Colonoscopy

NCT07587970 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1617

Last updated 2026-05-14

No results posted yet for this study

Summary

Through a multicenter, three-arm randomized controlled trial design, this study aimed to compare the effects of three positioning strategies-side-lying with elevated head position, supine with elevated head position, and standard side-lying position-on the incidence of hypoxemia during the recovery phase in patients undergoing painless gastroscopy and colonoscopy. The goal was to provide clinicians with a simple, non-invasive, and cost-effective optimization strategy.

Conditions

  • Postoperative Hypoxemia

Interventions

PROCEDURE

lateral decubitus head-up position (LH group)

An angle measuring device is placed beside the head of the examination bed to facilitate precise adjustment of the head position. Upon admission to the recovery room, the patient's Ramsay Sedation Scale score is assessed by an independent investigator (the attending anesthesiologist): 1 = agitated; 2 = fully awake, calm and cooperative; 3 = drowsy but responsive to verbal commands; 4 = drowsy but responsive to touch or pain; 5 = asleep but slow to respond to touch or pain; 6 = deep sleep with no response. Patients scoring 2-4 are immediately randomized into the study group, while those below this range are randomized after achieving the required score. Prior to enrollment, all patients remain in the left lateral position (bed head elevated 0°, consistent with the examination position). Patients assigned to the lateral supine head-elevated group (LH group) maintain their pre-assigned lateral position with the head elevated 30°.

PROCEDURE

supine head-up position (SH group)

An angle measuring device is placed beside the head of the examination bed to facilitate precise adjustment of the head position. Upon admission to the recovery room, the patient's Ramsay Sedation Scale score is assessed by an independent investigator (the attending anesthesiologist): 1 = agitated; 2 = fully awake, calm and cooperative; 3 = drowsy but responsive to verbal commands; 4 = drowsy but responsive to tactile or pain stimuli; 5 = asleep but slow to tactile or pain responses; 6 = deep sleep with no response. Patients scoring 2-4 are immediately randomized into the study group, while those below this range are randomized after achieving the required score. All patients are initially positioned in the left lateral decubitus position (head elevated at 0°, the same as during examination). Patients assigned to the supine head-elevated group (SH group) are transitioned from the lateral position to supine without a headrest, with the head elevated at 30°.

PROCEDURE

standard lateral decubitus position group (SL group)

An angle measuring device was placed beside the head of the examination bed to facilitate precise adjustment of the head position. Upon admission to the recovery room, the patient's Ramsay Sedation Scale was assessed by an independent investigator (the attending anesthesiologist): 1 = agitated; 2 = fully awake, calm and cooperative; 3 = drowsy but responsive to verbal commands; 4 = drowsy but responsive to touch or pain; 5 = asleep but slow to respond to touch or pain; 6 = deep sleep with no response. Patients scoring 2-4 were immediately randomized into the study group, while those below this range were randomized after achieving the required score. All patients were initially positioned in the left lateral decubitus position (head elevated at 0°, the same as during examination). Patients in the Standard Lateral Position Group (SL group) maintained their original left lateral position with the head elevated at 0°.

Sponsors & Collaborators

  • Yinchuan Traditional Chinese Medicine Hospital

    collaborator UNKNOWN
  • Guyuan Municipal People's Hospital

    collaborator UNKNOWN
  • Wuzhong City People's Hospital

    collaborator UNKNOWN
  • Zhongwei City People's Hospital

    collaborator UNKNOWN
  • Shizuishan City People's Hospital

    collaborator UNKNOWN
  • Zhongwei City Traditional Chinese Medicine Hospital

    collaborator UNKNOWN
  • Pingluo County People's Hospital

    collaborator UNKNOWN
  • Tongxin County People's Hospital

    collaborator UNKNOWN
  • Yanchi County People's Hospital

    collaborator UNKNOWN
  • Zhongning County People's Hospital

    collaborator UNKNOWN
  • Lingwu City People's Hospital

    collaborator UNKNOWN
  • Qingtongxia City People's Hospital

    collaborator UNKNOWN
  • General Hospital of Ningxia Medical University

    lead OTHER

Principal Investigators

  • Xinli Ni, Doctoral · 86-951-674-3252

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-12
Primary Completion
2026-12-31
Completion
2027-01-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07587970 on ClinicalTrials.gov