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Recovery Positions and Their Influence on Postoperative Hypoxemia in Pediatric Ambulatory Surgery: A Randomized Clinical Trial

Recovery Positions and Their Influence on Postoperative Hypoxemia in Pediatric Ambulatory Surgery: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119849
Enrollment
Unknown
Registered
2026-03-04
Start date
2026-03-04
Completion date
Unknown
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxemia

Interventions

Supine position group:The child maintained a supine position after entering the anesthesia recovery room.
Lateral position group:The child maintained a lateral position after entering the anesthesia recovery room.

Sponsors

kunming children's hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age: 1 - 12 years old. 2. ASA classification: Grade I - II. 3. No obvious cardiac or pulmonary dysfunction. 4. Children who need to undergo surgery under general anesthesia for day surgery will be transferred to the recovery room after the operation. 5. Voluntary participants in the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Body Mass Index (BMI) > 35 [BMI = weight (kg) / height (m)^2]. 2. Preoperative presence of bradycardia (heart rate < 50 beats/minute), hypotension (systolic blood pressure < 80 mmHg), or hypoxemia. 3. Requires long-term or intermittent oxygen inhalation due to pre-existing diseases. 4. Comorbid with diseases that cannot tolerate a decrease in arterial blood oxygen saturation or fluctuations in arterial blood carbon dioxide partial pressure (PaCO2), such as severe cardiovascular and cerebrovascular diseases, intracranial hypertension, or severe pulmonary diseases. 5. Coagulation dysfunction or a tendency to nosebleeds. 6. Patients unable to change their body position. 7. Participated in other intervention-based clinical studies within the past 3 months. 8. Other conditions judged by the researcher as not suitable for inclusion. 9. Patients or their families do not consent to participate in the study.

Design outcomes

Primary

MeasureTime frame
Hypoxemia;

Secondary

MeasureTime frame
Airway intervention measures;Hypoxia saturation level;Hypoxemia duration;The incidence of severe hypoxemia;Adverse reactions of cardiovascular system, respiratory system and digestive system ( including SpO2 decrease, hypotension, hypertension, bradycardia, tachycardia, new arrhythmia, nausea and vomiting .;Recovery time;

Countries

China

Contacts

Public ContactLiming Cheng

kunming children's hospital

medcheng@163.com+86 138 8876 4840

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026