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To examine the impact of SIMV ventilation mode on extubation outcomes and respiratory function in patients recovering from thoracoscopic lobectomy under general anesthesia

To examine the impact of SIMV ventilation mode on extubation outcomes and respiratory function in patients recovering from thoracoscopic lobectomy under general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112316
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-01-27
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Extubation response and respiratory function during anesthesia recovery and extubation

Interventions

Experimental group (SIMV):The experimental group (group S) was given SIMV mode of two-lung ventilation (TLV) immediately after drug withdrawal: FiO2 was 60%, tidal volume was 8ml/kg, frequency was 12-
Control group (VCV):The control group received two-lung ventilation with VCV mode, FiO2 was 60%, oxygen flow was 2L/min, tidal volume was 8ml/kg, respiratory rate was 12-16 times /min, I:E=1:2. The re

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists grade II-III; 2. Both sexes, aged from 18 to 65 years old; 3. body mass index (BMI) : 18.5-24.9 kg/m^2; 4. There were no obvious abnormalities in heart, brain, lung and endocrine function before operation.

Exclusion criteria

Exclusion criteria: 1. Preoperative mental disorders and inability to cooperate with patients; 2. There were anatomical abnormalities of the respiratory tract before operation; 3. Patients with preoperative asthma, chronic obstructive pulmonary disease, pulmonary infection and upper respiratory tract in the last two weeks; 4 Uncontrolled severe hypertension before surgery (SBP > 180 mmHg, DBP > 100 mmHg at rest); 5. Patients who were allergic to anesthetic drugs during operation or did not follow the established anesthesia scheme; 6. Patients with unexpected difficulty in intubation and ventilation of double-lumen bronchial tube during operation; 7. Intraoperative conversion to thoracotomy; 8. Patients with SpO2 < 95% (FiO2 100%) before setting the ventilation mode during the recovery period; 9. Patients with severe hemodynamic fluctuations requiring vasoactive drug intervention before setting ventilation mode during recovery period.

Design outcomes

Primary

MeasureTime frame
Incidence and classification of cough during extubation;

Secondary

MeasureTime frame
Systolic blood pressure;Diastolic blood pressure;Mean arterial pressure;Heart rate;Pulse oximetry;Partial pressure of oxygen;Carbon dioxide partial pressure;Index of oxygenation;Incidence of man-machine confrontation;Incidence of agitation and RASS score;The time of spontaneous breathing;Time to extubation;Length of PACU stay;Aldrete quality of recovery score;VAS score;

Countries

China

Contacts

Public ContactHongxing Min

General Hospital of Ningxia Medical University

minhongxing@126.com+86 137 0951 8969

Outcome results

None listed

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