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NCT03482076 Clinical Trial

Iron Deficiency Anemia in Childern With Liver Cirrhosis

Liver Cirrhosis Clinical Trial

— IDA  

Official title:
Prevelance of Iron Deficiency Anemia in Liver Cirrhosis in Childern

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03482076
Other study ID # DBK
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 23, 2018
Last updated March 23, 2018
Start date March 1, 2019
Est. completion date June 1, 2020

Study information
Verified date March 2018
Source Assiut University
Contact Bahaa Khaled Mohamed
Phone +201002755105
Email drbahaakhaled@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Iron deficiency anemia is a common complication of liver cirrhosis in childern and may affects there life this study to improve the outcome of these patients

Description:

Patients with cirrhosis are at risk of developing both IDA and anemia of chronic disease concomitantly, and there adverse effects can deteriorate general condition and affect of quality of life in these patients .Also because it is easier to correct IDA than anemia of chronic disease, so this study of the prevalence of IDA helping us in the diagnosis and treatment of IDA and can reduce the need for other diagnostic tests and improve the quality of life in patients with cirrhosis .

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date June 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Month to 18 Years
Eligibility Inclusion Criteria:

- all childern with liver cirrhosis in GIT and hepatology unit

Exclusion Criteria:

- Neonates less than one month

- childern with other liver diseases

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• transferrin receptor concentration
Sandwich radio-imunoassay

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary Prevelance of IDA in liver cirrhosis To evaluate results two years
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