Clinical study of clustering strategy to prevent perioperative lung complications in patients with craniofacial surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100042081

Enrollment

Unknown

Registered

2021-01-13

Start date

2021-01-20

Completion date

Unknown

Last updated

2021-04-19

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

Conditions

postoperative pulmonary complications

Interventions

Experimental group:Perioperative clustering intervention strategy

Control group :Routine diagnosis and treatment process during perioperative period

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form; 2. Patients with medium and high risk of perioperative pulmonary complications (ARISCAT score >= 26 points); 3. There is no abnormality in chest imaging before operation; 4. No mental disorder.

Exclusion criteria

Exclusion criteria: 1. Patients who have received lung surgery in the past; 2. Patients with COPD, asthma or apnea syndrome; 3. Patients with thoracic and intrathoracic diseases (mediastinal mass, chest tumor, etc.); 4. Patients with with severe neuromuscular diseases; 5. Patients who have used immunosuppressants and hormones in large quantities for a long time.

Design outcomes

Primary

Measure	Time frame
rate of complications after surgery;	—

Countries

China

Contacts

Public ContactSun Yongxing

Sanbo Brain Hospital, Capital Medical University

8793705@163.com+86 13521697866

Outcome results

None listed

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