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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03804398
Other study ID # FujianUnionAnethesiaOne
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 14, 2018
Est. completion date November 1, 2018

Study information

Verified date January 2019
Source Fujian Medical University Union Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To observe the effect of compliance guided an optimal Positive End-Expiratory Pressure(PEEP)on arterial oxygenation and intrapulmonary shunt during one-lung ventilation(OLV),and discuss the lung protective effect of optimal PEEP during one-lung ventilation.


Description:

Sixty patients undergoing thoracic surgery were randomly allocated to the study or control group.Patients were monitored for electrocardiogram, pulse oximetry, and non-invasive blood pressure,20 gauge cannula needle for radial artery catheterization under local anesthesia, monitoring ABP.,the right subclavian vein was selected for catheterization under local anesthesia,monitoring CVP.Anesthesia was induced with sufentanil 0.4 μg/kg, propofol 2 mg/kg, and cisatracurium 0.3 mg/kg.The trachea was intubated with a double-lumen tube (DLT),37F for male and 35F for female patients.Tube position was confirmed by bronchoscopy in the supine and lateral positions.Anesthesia was maintained with sevoflurane 1.0-1.5 vol%,propofol 2-4 mg/(kg·h) and remifentanil 0.1-0.2 μg/(kg·min) and intermittent cisatracurium 0.06-0.1 mg/kg.The lungs were initially ventilated using a volume-controlled ventilation mode,two-lung ventilation(TLV):tidal volume (VT) 8 ml/kg,respiratory rate 12-14 bpm, inspiratory:expiratory (I:E) ratio 1:2, in 60% oxygen without PEEP. During OLV, VT was reduced to 6 ml/kg,OLV was initiated at the moment of skin incision.Both groups received an alveolar recruitment maneuver(increase inspiratory pressure to 30cmH2O for 10s) at the 10min after one-lung ventilation. After the alveolar recruitment maneuver,the study group titrate PEEP from 4cmH2O,increased in 2cmH2O steps and hold at each step for 1min,and the static pulmonary compliance(Cst) would be record.Optimal PEEP was determined until the maximal static pulmonary compliance was obtained.In the control group at PEEP level of 5 cmH2O was established and maintained during the study period.Blood gas analyses, respiratory variables, and hemodynamic variables were recorded at 6 different time points:10 min after TLV(T0), 10min after OLV(T1), 30min after PEEP(T2), 60min after PEEP(T3), 10min after the end OLV(T4) and 20min after extubation(T5).


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date November 1, 2018
Est. primary completion date October 11, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Aged 18 yr to 65 yr

- Body mass index(BMI)18-28kg/m2

- American Society of Anesthesiologists Physical Status Classifications I to II

- Normal cardiac and pulmonary function

- Diagnosed with uncomplicated lung cancer and was to receive video-assist thoracoscopic lobectomy under general anesthesia.

Exclusion Criteria:

- Forced expiratory volume at one second/forced vital capacity <70%

- Asthma

- Chronic obstructive pulmonary disease

- Acute lung infection

- Past history of thoracic surgery

- Cardiac,hepatic,renal and endocrine diseases

- Preoperative glucocorticoid medication

- Preoperative chemotherapy

- Peripheral oxygen saturation(SpO2) kept below 90% for more than 10 minutes during operation

- Blood transfusion during operation

- Duration of one-lung ventilation less than an hour

- Occurrence of severe complications like allergic shock

Study Design


Related Conditions & MeSH terms


Intervention

Device:
compliance guided an optimal Positive End-Expiratory Pressure
The study groups received an alveolar recruitment maneuver(increase inspiratory pressure to 30cmH2O for 10s) at the 10min after one-lung ventilation. After the alveolar recruitment maneuver,the study group titrate PEEP from 4cmH2O,increased in 2cmH2O steps and hold at each step for 1min,and the static pulmonary compliance(Cst) would be record.Optimal PEEP was determined until the maximal static pulmonary compliance was obtained.
PEEP level of 5 cmH2O
In the control group at PEEP level of 5 cmH2O was established and maintained during the study period

Locations

Country Name City State
China FujianUnionHospital Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
Fujian Medical University Union Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary arterial oxygenation To observe the effect of compliance guided an optimal Positive End-Expiratory Pressure(PEEP)on arterial oxygenation 24 hours
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