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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04981990
Other study ID # Anesth
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2021
Est. completion date August 25, 2021

Study information

Verified date August 2021
Source Ain Shams University
Contact Esraa Abdellatif
Phone 01119895491
Email esraa301993@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hypoxia in single lung ventilation versus two lung ventilation in video assisted lung surgeries


Description:

Incidence of hypoxia in single lung ventilation by double lumen endotracheal tube "of choice in lung surgeries" versus incidence of hypoxia in two lung ventilation by conventional single lumen endotracheal tube "intermittent two lung ventilation"


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date August 25, 2021
Est. primary completion date August 25, 2021
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Age group: Adult patients from age of 21 years to 60 years - Sex: Both sexes - ASA Classification: patients with ASA classification II, III. - Elective lung surgeries using video assisted thoracoscopic surgeries. Exclusion Criteria: - Patients refuse to give informed consent. - ASA Classification: ASA IV. - Failure of thoracoscopic surgeries and continue as open thoracotomy - Patients with ischemic heart diseases, where hypoxemia might be preexisting, or patient be more vulnerable to hypoxemia whatever the technique or time of hypoxia. - Emergency lung surgeries. - Patients underwent previous lung surgeries of any cause. - Patients with pathology to the non-operated side.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Single lung ventilation by double lumen endotracheal tube
Single lung ventilation using double lumen endotracheal tube and isolation of the operated lung during surgery to create ideal surgical field
Two lung ventilation by conventional single lumen endotracheal tube
Intermittent two lung ventilation so that no significant hypoxia occurs with creating optimum surgical field

Locations

Country Name City State
Egypt Aun Shams University Hospitals Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of hypoxemia Hypoxemia in single and two lung ventilation by serial arterial blood gases Intraoperative to first 24 hours post operative
Secondary Incidence of failure to correct Hypoxemia in single lung ventilation Stop lung isolation and procedure using two lung ventilation to correct hypoxia Intraoperative
Secondary Incidence of failure of two lung ventilation to create optimum surgical field Frequent stopping of ventilation and the surgent can't access the surgical field easily Intraoperative
Secondary Incidence of post operative complications Any associated complications First 24 hours post operative
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