Effect of SARS-CoV-2 infection on perioperative respiratory complications in patients undergoing elective oral surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300068052

Enrollment

Unknown

Registered

2023-02-06

Start date

2023-02-06

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

General anesthesia Postoperative pulmonary complications SARS-CoV-2 infection

Interventions

1 month after healing of covid-19 infection:None

2 month after healing of covid-19 infection:None

Eligibility

Sex/Gender

All

Age

6 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients more than 2 weeks after the disappearance of symptoms of SARS-CoV-2; 2. 1 year <= age <= 90 years; gender not limited; 3. Patients with ASA scores I~III; 4. Willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Preoperative antigen-positive patients; 2. With severe systemic disease ASA grade III or higher; 3. Drug allergy or surgical intolerance; 4. Patients who are pregnant or lactating; 5. Chest radiograph/CT showing active inflammation on the lungs; 6. Myocardial enzyme profile results showing severe myocardial damage; 7. Inability to cooperate with the study for any reason.

Design outcomes

Primary

Measure	Time frame
forced vital capacity;forced expiratory volume in one second;Pulmonary Function Tests;	—

Secondary

Measure	Time frame
Postoperative respiratory adverse reactions;	—

Countries

China

Contacts

Public ContactSisi Li

Stomatological Hospital Affiliated to Chongqing Medical University

500940@hospital.cqum.edu.cn+86 152 2334 0305

Outcome results

None listed

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