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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02534025
Other study ID # 1/2015
Secondary ID
Status Recruiting
Phase N/A
First received August 9, 2015
Last updated February 5, 2017
Start date January 2016
Est. completion date March 2017

Study information

Verified date February 2017
Source Mansoura University
Contact AlRefaey Kandeel, MD
Phone +201008158591
Email refa3ey2@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Remote (upper arm) ischemic preconditioning in the donor of living donor liver transplanta to ameliorate the effect of reperfusion injury in recipients.


Description:

Upper arm ischemia will be induced by elevation of NIBP cuff pressure to 200 mm Hg for 5 minutes repeated four times 5 mniutes apart, aiming to decrease the effect of ischemia reperfusion in the graft liver.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria:

- All candidates for living donor liver transplantation

Exclusion Criteria:

- Donors with peripheral vascular disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ischemia preconditioining
Elavate blood pressure cuff pressure to 200

Locations

Country Name City State
Egypt Mansoura university Mansoura Dkahleya

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary liver enzymes ( SGOT and SGPT) as indicator of graft injury Hemodynamic effects of reperfusion ijury 30 minutes