The impact of Autoflow mode of mechanical ventilation on postoperative atelectasis in infants: a randomized, double-blinded, three-arm, controlled trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000034122

Enrollment

Unknown

Registered

2020-06-24

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-06-29

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

Conditions

postoperative atelectasis

Interventions

Group 1:Autoflow mode

Group 2:volume control ventilation

Group 3:pressure control ventilation

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Elective ventriculoperitoneal shunt under general anesthesia; (2) Age: 0-1 year; (3) ASA physical status: I-II.

Exclusion criteria

Exclusion criteria: (1) Obvious cardiovascular diseases; (2) Obvious respiratory disease such as bronchopulmonary dysplasia; (3) Upper respiratory tract infection within two weeks; (4) Refusal to participate by a guardian; (5) Already participated in other clinical trials.

Design outcomes

Primary

Measure	Time frame
incidence of atelectasis at the end of operation;	—

Secondary

Measure	Time frame
atelectasis score at the end of operation;PaO2;PaO2/FiO2;mean inspiratory pressure;	—

Countries

China

Contacts

Public ContactLinlin Song

Peking University First Hospital

songlinlinlynkia@163.com+86 13501309217

Outcome results

None listed

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