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NCT04106323

A Study of Factor Inhibitors in Adult Patients With Hemophilia and Von Willebrand's Disease in Upper Egypt

Status unknown Last updated 12 March 2020
What this trial tests

trial in Hemophilia in 100 participants. Status unknown.

Timeline
10 May 2020
Primary endpoint
10 November 2020
20 August 2021

Quick facts

Lead sponsorSafaa AA Khaled
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date10 May 2020
Primary completion10 November 2020
Estimated completion20 August 2021

Conditions studied

Sponsor

Safaa AA Khaled — full company profile →

Who can join

Adults 18 to 55, any sex, with Hemophilia or Von Willebrand Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hemophilia A and B are bleeding disorders caused by deficiency of factor VIII and IX, respectively. The deficiency of one of these coagulation factors is due to a mutation on the X chromosome. Accordingly replacement of the deficient factor is currently the main treatment for these disorders. The most disappointing complication of replacement therapy in hemophilia is the development of inhibitors. Unlike haemophilia , inhibitor development in patients with V Willebrand's Disease (VWD) is a rare complication of treatment. Studies on inhibitors whether on hemophilia or VWD are limited in our region. This study aims to 1. To estimate the frequency of factor inhibitors in hemophilia and VWD patients in our region. 2. To investigate modifiable risk factors associated with development of inhibitors in both diseases. 3. To correlate the level of inhibitor with the clinical presentation of the patients. 4. To assess influence of factor inhibitors on quality of life in patients who developed factor inhibitors in both diseases.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hemophilia

Currently open trials in the same condition.

Other Safaa AA Khaled trials

Trials by the same sponsor.

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Data sources for this page

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