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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05381701
Other study ID # 2020/25-6
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date December 31, 2021

Study information

Verified date May 2022
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of atelectasis that may be caused by different flow rate anesthesia applications during the operation with lung ultrasound score.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - operation time 2-5 hours - elective septoplasty and rhinoplasty - ASA I-II Exclusion Criteria: - morbid obesity - malignant hyperthermia - opioid sensitivity - alcohol or drug addiction - congestive heart failure - chronic obstructive pulmonary disease - coronary artery disease - anemia - liver and kidney diseases - pregnancy - breast-feeding - history of allergy to drugs used

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Lung Ultrasound Score
Measuring the atelectasis area by ultrasound guidance from 12 different regions of the lung

Locations

Country Name City State
Turkey Zonguldak Bülent Ecevit University Faculty of Medicine Zonguldak Kozlu

Sponsors (1)

Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary assessment of lung ultrasound score Effect of different flow anesthesia on lung ultrasound score Change from Baseline and 30 minute after emergence
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