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A randomized controlled study evaluating the effects of protective lung ventilation strategies on postoperative pulmonary and cognitive function in patients undergoing orthopedic surgery with tourniquets

A randomized controlled study evaluating the effects of protective lung ventilation strategies on postoperative pulmonary and cognitive function in patients undergoing orthopedic surgery with tourniquets

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058701
Enrollment
Unknown
Registered
2022-04-14
Start date
2022-04-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

protective lung ventilation

Interventions

The control group:Set tidal volume to 10 ml/kg, inhaled oxygen concentration (FiO2) 100% during anesthesia induction and double lung ventilation, without end-expiratory positive pressure (PEEP)
test group 1:The tidal volume is set to 6~8ml/kg, the positive pressure at the end of expiratory breath (PEEP) is 3 to 5 cmH2O, and the inhaled gas oxygen concentration (FiO2) during anesthesia induct
test group 2:The tidal volume is set to 6~8ml/kg, the positive end-expiratory pressure (PEEP) is 3~5cmH2O, and the inhalation gas oxygen concentration (FiO2) during anesthesia induction and double lun
test group 3:The tidal volume is set to 6 to 8 ml/kg, the positive pressure at the end of breath (PEEP) is 3 to 5 cmH2O, and the inhaled gas oxygen concentration (FiO2) during anesthesia induction and

Sponsors

The Third Affiliated Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I or II; 2. Aged 18-85; 3.BMI 18-28 kg/m2; 4. No history of anemia and hypoproteinemia; 5. No history of chronic pain, central nervous and psychological diseases, antidepressants and sedatives, Parkinson's disease and epilepsy; 6. No history of hypoxemia, chronic obstructive pulmonary disease (COPD), other chronic pulmonary diseases and asthma before operation; 7. No obvious organic diseases such as brain, heart, lung, liver and kidney.

Exclusion criteria

Exclusion criteria: 1. preoperative MMSE score 4h, bleeding volume > 800ml; 11. The tourniquet has been used for more than 1.5 hours; 12. Those who do not agree to participate in the study.

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure, diastolic blood pressure, mean arterial pressure, heart rate, respiratory rate, blood oxygen saturation;PaO2, PaCO2, SaO2, Lac and calculated PaO2/FiO2 and intrapulmonary shunt rate Qs/Qt, alveolar artery oxygen partial pressure difference (PA-aDO2);Tidal volume (VT), lung compliance (Cdyn), peak airway pressure (PEAK), mean airway pressure (Pmean), plateau pressure (PLAT), airway resistance (Raw);Inflammatory indicators of the blood;The patient's mental state was assessed by MMSE score before surgery, and the postoperative cognitive function on the 1st and 3rd day after surgery was followed up to assess the cognitive function on the 1st and 3rd days after surgery;Record the time of tourniquet use, surgery time, anesthesia time, in and out, and underlying disease.;

Countries

China

Contacts

Public ContactWang Qiujun

The Third Affiliated Hospital of Hebei Medical University

13933178001@163.com+86 18533112929

Outcome results

None listed

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