Effect of Postural Changes on Postoperative Hypoxemia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorYuhu Ma

About this trial

The goal of this clinical trial is to learn which positioning strategy works better to prevent postoperative hypoxemia in surgical patients: semirecumbent positioning or lateral positioning. It will also learn about the safety and effectiveness of these two positioning approaches. The main questions it aims to answer are:

Does semirecumbent positioning reduce the incidence of postoperative hypoxemia more effectively than lateral positioning? Does lateral positioning reduce the incidence of postoperative hypoxemia more effectively than semirecumbent positioning? What are the differences in patient comfort and recovery outcomes between these two positioning strategies? Researchers will compare semirecumbent positioning directly to lateral positioning to see which approach is more effective in preventing postoperative hypoxemia.

Participants will:

Be randomly assigned to either semirecumbent positioning or lateral positioning after surgery Have their oxygen levels and breathing monitored regularly during the postoperative period Receive standard post-surgical care with their assigned positioning strategy Be assessed for comfort levels and any positioning-related complications Have their recovery progress tracked throughout their hospital stay.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18 or above and 80 or below who received general anesthesia and intubation

Disqualifiers

Presence of hypotension or bradycardia upon entering the anesthesia recovery room;

Preoperative hypoxemia;

Surgical procedures where body position adjustment is not possible or is prohibited due to the nature of the surgery;

Surgical procedures involving severe cardiovascular or cerebrovascular diseases, severe pulmonary diseases, intracranial hypertension, etc.;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Lateral positioning

    Behavioral

    Patients allocated to lateral positioning were placed at 90° on a horizontal bed, supported with a pillow to maintain neutral alignment of the spine and avoid hyperextension or forward flexion of the neck. No preference was specified for left or right lateral decubitus positioning, allowing flexibility based on patient comfort and surgical requirements.

  • Semirecumbent positioning

    Behavioral

    Patients in the semi-recumbent position were placed in the bed and the head of the bed was raised by 30 °, allowing flexibility based on patient comfort and surgical requirements.

Treatment groups

1,200 Participants
are divided into 2 treatment groups
Group A: Semirecumbent positioningExperimental treatment 1 intervention
Group B: Lateral positioningExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Incidence of hypoxaemia

Defined as any occurrence of oxygen saturation (SpO2) ≤90% for at least five seconds during the initial 10 minute period after positioning.

Time frame
Within 24 hours after the surgery was completed

Secondary outcomes

1

Rrequency of airway rescue interventions

Increased oxygen flow, jaw thrust manoeuvre, mask ventilation

Time frame
Within 24 hours after the surgery was completed
2

incidence of severe hypoxaemia

oxyhemoglobin saturation ≤85%

Time frame
Within 24 hours after the surgery was completed
3

Lowest oxygen saturation

Defined as the oxygenation nadir during 10 minutes of continuous measurement.

Time frame
Within 24 hours after the surgery was completed
4

Duration of stay in the post-anaesthesia care

Duration of stay in the post-anaesthesia care

Time frame
Perioperative/Periprocedural

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Yuhu Ma

Lead sponsor

LanZhou University

Sponsor institution

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