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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04373174
Other study ID # BYIERH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date May 15, 2021

Study information

Verified date January 2023
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Today, it is preferred that the lung with pathology for thorax surgery is not under ventilation during operation in terms of reliability and ease of operation. For this reason, the anesthesia approach is characteristic and it is ensured that the single lung is not ventilated during the operation by means of specially manufactured intubation tubes. This application can disrupt tissue oxygenation due to both Operation position and single lung ventilation. Thoracic epidural analgesia, which is applied as the gold standard of Thoracic Surgery, is applied prior to the operation and is provided to assist in postoperative analgesia.


Description:

The aim of this study was to investigate the effect of thoracic epidural analgesia method on brain tissue oxygenation in patients with single lung ventilation.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 15, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients who were in the American Society of Anesthesiologists (ASA) I-III class - Underwent Thoracic Surgery Exclusion Criteria: - Local anesthetic allergy, - Bleeding is a diathesis disorder - Allergic to the drugs used, - Patients who are not reluctant to participate in the study, - Presence of infection in the block area, - Patients whose body mass index is over 30

Study Design


Intervention

Device:
Regional oximetry probe
Regional oximetry probe will be placed in the frontal area of the head
Procedure:
Thoracic Epidural block
Thoracic epidural block will be applied to the patients before the operation begins

Locations

Country Name City State
Turkey Bursa Yuksek Ihtisas Training and Research Hospital Bursa

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary rso2 Regional oximetry probe will be placed in the frontal area of the head peroperative 2 hours
Secondary po2 Arterial blood gas oxygen pressure peroperative 2 hours
Secondary ETCO2 End-tidal carbon dioxide (ETCO2) level peroperative 2 hours
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