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NCT Number: NCT07673042

Effect of Preoxygenation Position and Examination Position on Hypoxemia During Painless Gastrointestinal Endoscopy

To investigate the independent effects and interaction of pre-oxygenation position (left lateral vs left lateral with 30° head-up tilt) and examination position (left lateral vs left lateral with 30° head-up tilt) on hypoxemia during painless gastroscopy and colonoscopy using a 2×2 factorial design.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

General hospital of Ningxia medical university

Yinchuan, Ningxia, 750001, China

Location contact

xiaoyong wei, Master's degree

CONTACT

[email protected]

86-951-674-3252

About this study

Painless gastroscopy and colonoscopy represent core minimally invasive techniques for colorectal cancer screening and the diagnosis and treatment of gastrointestinal diseases. By utilizing intravenous sedation to ensure a pain-free experience, these procedures are widely adopted in clinical practice. However, perioperative hypoxemia remains the most common and critical safety complication during sedation for endoscopy. It is primarily caused by anesthesia-induced respiratory depression, tongue base collapse, airway obstruction, diaphragmatic compression, and restricted thoracic movement, with significantly elevated risks observed in obese, elderly, snoring, and short-necked patients.

Hypoxemia may trigger bradycardia, arrhythmias, myocardial ischemia, and cerebral hypoxia. In severe cases, it can lead to apnea, laryngospasm, and forced termination of the procedure, making it a key indicator in endoscopic anesthesia quality control.

Pre-oxygenation is a fundamental measure to increase functional residual capacity (FRC) and prolong the safe apneic time prior to induction, thereby preventing hypoxemia. The examination position directly determines airway patency, mandibular relaxation, diaphragmatic position, and thoracic compliance throughout the procedure. Both are critical, controllable factors regulating perioperative oxygenation. Studies have confirmed that the left lateral position reduces the incidence of hypoxemia, while the left lateral position with 30° head elevation effectively relaxes the mandible, alleviates tongue base collapse, reduces abdominal organ pressure on the diaphragm, and improves ventilation and oxygenation by increasing FRC.

Current research largely focuses on either the pre-oxygenation position or the examination position in isolation, presenting notable limitations: first, the interaction between these two positions has not been evaluated, leaving the synergistic or antagonistic effects of combined interventions unclear; second, there is a lack of efficient validation using a factorial design, which is necessary to simultaneously analyze the main effects and interactions of both independent variables.

Addressing these clinical challenges and research gaps, this study employs a 2×2 factorial randomized controlled design. With pre-oxygenation position and examination position serving as the two intervention factors, the study aims to explore the individual and combined effects of both factors on perioperative hypoxemia. The objective is to identify the optimal positional combination, establish standardized and generalizable positioning protocols for painless endoscopy, accurately reduce the incidence of hypoxemia, enhance the precision of anesthesia management, and provide high-level evidence to guide clinical practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 to 75 years, regardless of gender
  • Body mass index (BMI): 18.5 - 35 kg/m²
  • ASA physical status class I, II or III
  • Scheduled for painless gastroscopy, painless colonoscopy, or combined painless gastroenteroscopy
  • Able to understand the study procedure and provide written informed consent

Exclusion criteria

  • Severe cardiopulmonary diseases, including severe COPD, heart failure, severe arrhythmia and pulmonary hypertension
  • Difficult airway identified before anesthesia
  • Severe obstructive sleep apnea (OSA)
  • Spinal or thoracic deformity
  • Preoperative baseline hypoxemia
  • Known allergy to any anesthetic drugs used in this study
  • Pregnant females
  • Unable to cooperate with required intraoperative body position

Treatment and study plan

Pre-oxygenation Position (left lateral position)

Procedure

An angle measuring device is placed beside the head of the examination bed to enable precise adjustment of the head position. Pre-oxygenation phase: Administer pure oxygen via a standardized mask with tight fit, at a flow rate of 6 L/min; instruct the patient to take deep breaths while receiving continuous oxygen for 3 minutes, maintaining the same body position throughout. If the position is altered during this phase, discontinue the procedure. Left lateral pre-oxygenation: The patient assumes a left lateral position on a horizontal bed surface with the head elevated at 0°, supported by pillows to maintain a neutral spine position and avoid excessive neck extension or flexion.

Other names: left lateral position

Examination Position(left lateral position )

Procedure

Examination Phase: From the initiation of anesthesia and endoscope insertion until completion of the procedure, the patient's position and head-of-bed angle must remain fixed throughout; any adjustments are prohibited during this phase. If the position is altered midway through the examination, the patient will be excluded from the study. Left lateral position examination: The patient assumes a 90-degree left lateral position on a horizontal bed surface with the head of the bed elevated to 0°, supported by pillows to maintain a neutral spinal alignment, avoiding excessive neck extension or flexion.

Other names: Left lateral position

Pre-oxygenation Position( left lateral head elevation in a 30-degree position)

Procedure

An angle measuring device is placed beside the head of the examination bed to allow precise adjustment of the head position. Pre-oxygenation phase: The patient receives pure oxygen via a standardized mask with tight fit, at a flow rate of 6 L/min; they are instructed to take deep breaths while receiving continuous oxygen for 3 minutes, maintaining the same body position throughout. If the position is altered during this phase, the procedure is discontinued. Left-sided head elevation (30°): During pre-oxygenation, the patient lies in a left lateral position on a horizontal bed surface with the head elevated by 30°, supported by pillows to maintain a neutral spinal alignment and prevent excessive neck extension or flexion.

Other names: left lateral head elevation in a 30-degree position

Examination Position(left lateral head elevation in a 30-degree position)

Procedure

Examination Phase: From the initiation of anesthesia and endoscope insertion until completion of the procedure, the patient's position and head-of-bed angle must remain fixed throughout; any adjustments are prohibited during this phase. If the position is altered midway through the examination, the patient will be excluded from the study. Left lateral decubitus examination: The patient assumes a left lateral position on a horizontal bed surface with the head elevated at 30°, supported by a pillow to maintain a neutral spinal alignment, avoiding excessive neck extension or flexion.

Other names: left lateral head elevation in a 30-degree position

Primary outcomes

  1. Incidence of hypoxemia

    Time frame: During procedure

    Incidence of SpO₂ ≤ 90% for >10 seconds during the examination.

Secondary outcomes

  1. Safe duration of pre-oxygenation

    Time frame: During procedure

    Time from cessation of oxygen administration (start of anesthesia induction) to first SpO₂ <92% for ≥3 seconds. If no desaturation occurs, the value equals the duration from oxygen cessation to end of procedure (right-censored).

  2. Incidence of subclinical respiratory depression

    Time frame: During procedure

    Defined as the proportion of participants experiencing SpO₂ between 90% and 95% (inclusive) at any time during the examination.

  3. Requirement for jaw thrust

    Time frame: During procedure

    Number of participants requiring manual jaw thrust to relieve airway obstruction during the examination.

  4. Requirement for nasal cannula oxygen

    Time frame: During procedure

    Number of participants requiring oxygen supplementation via nasal cannula during the examination.

  5. Requirement for increased oxygen flow

    Time frame: During procedure

    Number of participants requiring an increase in oxygen flow rate during the examination.

  6. Requirement for mask ventilation

    Time frame: During procedure

    Number of participants requiring bag-mask ventilation during the examination.

  7. Requirement for endotracheal intubation

    Time frame: During procedure

    Number of participants requiring endotracheal intubation during the examination.

  8. Incidence of airway intervention

    Time frame: During procedure

    Proportion of participants requiring any airway intervention (jaw thrust, nasal cannula, increased flow, mask ventilation, or intubation)

  9. Severity of coughing

    Time frame: During procedure

    Assessed using a 4-grade scale: Grade I (none), Grade II (single mild episode), Grade III (multiple episodes <15s), Grade IV (continuous >15s)

  10. Length of stay in recovery room

    Time frame: Up to 30 minutes post-anesthesia care unit (PACU) admission

    Time from arrival to discharge from the recovery room (maximum observation 30 minutes)

  11. Endoscopist satisfaction score

    Time frame: During procedure

    Assessed using a Numerical Rating Scale (NRS) ranging from 0 to 10, with higher scores indicating greater satisfaction.

  12. Incidence of postoperative nausea, vomiting, headache, and dizziness

    Time frame: Up to 30 minutes post-anesthesia care unit (PACU) admission

    Proportion of participants experiencing nausea, vomiting, headache, or dizziness after awakening in the recovery room.

Other outcomes

  1. Safety outcome endpoints:heart rate

    Time frame: Baseline and during procedure

    Recorded at T0 (before pre-oxygenation), T1 (before induction), T2 (scope insertion), and T3 (scope removal).

  2. Safety outcome endpoints:blood pressure

    Time frame: Baseline and during procedure

    Recorded at T0 (before pre-oxygenation), T1 (before induction), T2 (scope insertion), and T3 (scope removal)

  3. Safety outcome endpoints:peripheral oxygen saturation (SpO₂)

    Time frame: Baseline and during procedure

    Recorded at T0 (before pre-oxygenation), T1 (before induction), T2 (scope insertion), and T3 (scope removal).

  4. Safety outcome endpoints:Incidence of hemodynamic instability in recovery

    Time frame: Up to 30 minutes post-anesthesia care unit (PACU) admission

    Occurrence of tachycardia (>100 bpm), bradycardia (<50 bpm), or hypotension (systolic blood pressure <80 mmHg) during the recovery period.

Study contacts

Contact information is provided by the study sponsor or research team.

xiaoyong wei, Master's degree

CONTACT

[email protected]

86-951-674-3252

Sponsors and collaborators

Lead sponsor

General Hospital of Ningxia Medical University

Other

Registry information

Official study title

Effect of Preoxygenation Position and Examination Position on Hypoxemia During Painless Gastrointestinal Endoscopy: A 2×2 Factorial Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 29, 2026
Registry last updated
Jun 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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