Respiratory Complications Among Living Liver-donors

Complication of Anesthesia Clinical Trial

Official title:

Respiratory Complications Among Living Liver-donors: a Single Center Observational Retrospective Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03862664
• Other study ID #: FAMSU R37/2018
• Status: Active, not recruiting
• Start date: February 6, 2019
• Est. completion date: May 2019

Study information

• Verified date: February 2019
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Recently, there are increasing reports about pulmonary complications within living liver donors postoperatively. In this retrospective study, the investigators will highlight the risk factors and incidence of pulmonary complication among living liver-donors in our center.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 124
• Est. completion date: May 2019
• Est. primary completion date: April 2019
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

• Excellent general physical and mental condition,

• Free of chronic disease or

• Previous major abdominal surgery,

• Body mass index (BMI) <28,

• ABO blood group identical to recipients and

• Negative for hepatitis B, C and human immunodeficiency viruses (HIV).

Exclusion Criteria:

• ASA physical status> II,

• BMI>28,

• Psychiatric or mental retardation,

• pregnant and nursing women or

• Patients with significant laboratory abnormalities

Related Conditions & MeSH terms

• Complication of Anesthesia

Intervention

Procedure:
• Collection of data
The investigators will retrieve retrospectively the medical record of donors who underwent hepatic lobectomy for liver transplantation

Locations

Country	Name	City	State
Egypt	Ain 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	The number of participants with postoperative respiratory complications	Respiratory complications as pulmonary embolism, pleural effusion, pneumothorax, pneumonia, atelectasis, acute lung injury (ALI), acute respiratory distress syndrome (ARDS), and transfusion-related acute lung injury (TRALI) will be considered when they are clinically evident.	an average period of 3 year
Secondary	The average of ICU stay among patients	It is defined as time period from entry to ICU till discharge to the ward	an average period of 3 year
Secondary	The average of hospital stay among patients	It is defined as time period elapsed from discharge to the ward till leaving the hospital	an average period of 3 year