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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06118489
Other study ID # HamidiyeKAEK-98172
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2023
Est. completion date February 1, 2024

Study information

Verified date October 2023
Source Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The bronchodilator effects of volatile anesthetics have been the subject of many clinical studies. It is known that all volatile anesthetics, especially halothane, have similar effects. Sevoflurane has been shown to reduce airway resistance more than halothane and isoflurane. Desflurane is difficult to use as an induction agent due to its harsh and extremely pungent odor and airway irritating effect. However, it has been shown that the risk of cough, respiratory arrest and laryngospasm is no different from sevoflurane when administered after intravenous induction. Although it irritates the airway, it is thought to have a bronchodilation effect as it stimulates the sympathetic system. In spinal surgeries, prone position is required to access the operating field. When the patient is placed in the prone position, pulmonary physiology are affected. In the prone position, V/Q mismatch decreases and arterial oxygenation increases. However, lung compliance decreases and the peak inspiratory pressure required to reach the required tidal volume increases. The main purpose of this study is the effect of volatile agents on lung mechanics and oxygenisation in the prone position.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date February 1, 2024
Est. primary completion date February 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18-65 years old - ASA1-2 - Patients planned to undergo spinal surgery Exclusion Criteria: - 1 - Lung disease - BMI 35 and above - Smokers - Those under the age of 18 and over the age of 65 - Hepatorenal disease - Reynaud's disease - Burger disease - Hypotensive patient - Neuromuscular disease - Those who have had thoracic surgery before - Those with bad Allen test results

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Yadigar Yilmaz Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary compliance pulmonary compliance before, during and after prone position 2 hour
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