Protective lung ventilation accelerate recovery of patients undergoing abnominal surgery: a single center randomised controlled trial

The clinical application research for protective lung ventilation in ehanced recovery after surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900024829

Enrollment

Unknown

Registered

2019-07-29

Start date

2019-09-01

Completion date

Unknown

Last updated

2019-08-27

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

Conditions

Postoperative pulmonary complications

Interventions

treated group:protective lung ventilation

control group:conventional ventilation

Eligibility

Sex/Gender

All

Age

50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients undergoing abnominal surgery; ASA grade 2-3; aged 51 to 80 years; no gender limit; no previous cardiac or pulmonary disease; BMI 18-25; the ARISCAT score more than 26.

Exclusion criteria

Exclusion criteria: 1.Anemia (Hb 45mmHg; 5.neuromuscular disease.

Design outcomes

Primary

Measure	Time frame
IL-6;IL-10;MDA;SP-A;ICAM;NF-kß;LUS;PPCs;	—

Countries

China

Contacts

Public ContactGao Yongtao

Affiliated Hospital of Nantong University

gyt19700114@sina.com+86 13962988003

Outcome results

None listed

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