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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02483806
Other study ID # 4-2015-0325
Secondary ID
Status Completed
Phase N/A
First received June 19, 2015
Last updated December 26, 2017
Start date June 29, 2015
Est. completion date May 25, 2016

Study information

Verified date December 2017
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

One lung ventilation (OLV) is essential during thoracic surgery. During OLV, intrapulmonary shunt can be increased resulting hypoxemia. Wang et al measured intrapulmonary shunt by transesophageal echocardiography. Although OLV technique had been advanced so far, hypoxemia during OLV reaches about 10% in spite of inspired oxygen fraction 100%. Applying PEEP(Positive End-expiratory Pressure) at dependent lung and CPAP at non-dependent lung can mitigate the hypoxemia. Above all, PEEP can be easily applicable. However, there are controversial studies whether it is supportive or not. In this prospective, cross-over study, the investigators are planning to investigate the effects of PEEP on intrapulmonary shunt, oxygenation and cardiac function as well.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date May 25, 2016
Est. primary completion date May 25, 2016
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- scheduled for VATS lobectomy

- 40 = age = 80

- American Society of Anaesthesiologists(ASA) physical status classification I~III

Exclusion Criteria:

- American Society of Anaesthesiologists(ASA) physical status classification IV

- NYHA class III~IV

- Severe obstructive lung disease and/or restrictive lung disease patients

- those with end-organ diseases (i.e. heart failure, respiratory failure, hepatic failure, renal failure)

- arrhythmia

- esophageal varix

- pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
PEEP
After induction of anesthesia, including insertion of TEE probe, change position from supine to lateral position. Measure ABGA and cardiac indices for the baseline value. Apply each PEEP (0, 5, 10 cmH2O) serially at the random order. 6 sequences (0->5->10, 0->10->5, 5->10->0, 5->0->10, 10->5->0, 10->0->5) are equally applied to 6 patients (total 6x6=36 patients) who agreed to this study. Measure ABGA and cardiac indices after 20 min at each step of peep apply(3 times).

Locations

Country Name City State
Korea, Republic of Department of Anaesthesiology and Pain Medicine, Anaesthesia and Pain Research Institute, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary the effect of differential PEEP (0, 5, 10 cmH2O) by PaO2(P/F ratio) 20 minutes after each PEEP apply
Primary Cardiac function cardiac function : Tei index 20 minutes after each PEEP apply
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