Completed

Causes of Disqualification of Egyptian Potential Living Liver Donors

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

From 18 to 50 Years
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: June 2010
See protocol details

Summary

Principal SponsorAin Shams University
Last updated: March 12, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: June 1, 2010

Actual date on which the first participant was enrolled.

The aim of this work is to identify and analyze the causes of disqualification of potential Egyptian living liver-donors in a University based liver transplant program

NCT01809249
Principal SponsorAin Shams University
Last updated: March 12, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

192 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 50 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: All potential living liver donors in the period from June 2010 to June 2012 Age between 18 and 50 years Relationship within 3rd degree of consanguinity with recipient or spouse. The donor-recipient pair must be blood group compatible. An informed consent should be obtained. Exclusion Criteria: Patients with nknown mrsdical or surgical history that interfere with donation Underlying medical condition (diabetes, cardiopulmonary disease, etc.). ABO incompatibility

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Ain Shams Center For Organ Transplantation (ASCOT),Ain Shams university

Cairo, EgyptOpen Ain Shams Center For Organ Transplantation (ASCOT),Ain Shams university in Google Maps
CompletedOne Study Center