Skip to content

Postanesthesia complications associated with airway management in children infected with SARS-CoV-2 in the early stage of rehabilitation: A controlled observational study

Postanesthesia complications associated with airway management in children infected with SARS-CoV-2 in the early stage of rehabilitation: A controlled observational study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069293
Enrollment
Unknown
Registered
2023-03-13
Start date
2023-03-13
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Novel coronavirus infectious disease (SARS-CoV-2)

Interventions

2 weeks after recovery group:None
3 weeks after recovery group:None
4 weeks after recovery group:None
5 weeks after recovery group:None
8 weeks after recovery group:None

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled tonsil adenoidectomy, sinus operation, appendix operation, inguinal hernia repair, circumcision, and other unlisted otorhinolaryngology, general surgery, thoracic surgery or orthopedic surgery; 2. Aged <=18 years; 3. ASA? or ? level; 4. Operation time is less than 2 hours and gender is not limited.

Exclusion criteria

Exclusion criteria: 1. Weight below or above the standard body weight ±15% [standard body weight (kg) = height (cm) -100]; 2. Children with asthma or airway hyperresponsiveness, neuromuscular systemic disease or cachexia; 3. Children with difficult airway; History of recovery from abnormal surgical anesthesia; 4. Severe acid-base imbalance, or severe electrolyte disturbance; 5. Children who had participated in any drug clinical trials within 30 days before the study began; 6. Heart surgery; 7. Other conditions deemed unsuitable for inclusion by the researchers.

Design outcomes

Primary

MeasureTime frame
Incidence of perioperative hypoxia;

Secondary

MeasureTime frame
Incidence of other adverse effects;Days in hospital;Parental stress;

Countries

China

Contacts

Public ContactShangguan Wangning

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

sgwning@163.com+86 135 8763 7891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026