Actively Recruiting

All Genders
NCT07218536

The Burden of Atypical Hemolytic Uremic Syndrome and The Clinical Characteristics of Patients in Egyptian Hospitals A Multicenter, Observational, Retrospective Cohort Study in Egypt

Led by AstraZeneca · Updated on 2026-04-16

200

Participants Needed

8

Research Sites

50 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Atypical hemolytic uremic syndrome (aHUS) is a rare, progressive, and life-threatening disease that occurs at any age, with incidence rate of 0.75 to 2.0 cases per million population per year. aHUS is a thrombotic microangiopathy (TMA) commonly caused by dysregulation of the complement system, affecting several organs, especially the kidneys. aHUS can be familial or sporadic, and approximately 50% to 60% of patients have specific identifiable genetic complement mutations and antibodies. Although aHUS is a rare disease, it has a significant impact on the quality of life because of its poor prognosis: a 25% global mortality rate; more than 50% of untreated patients advance to endstage renal disease (ESRD); and more than 75% of adults with renal failure require prompt dialysis. The risk of relapse is also high in many patients, either in the native or transplanted kidneys, so long-term management and close monitoring are essential. Advancements in aHUS therapies, especially the availability of anti-complement therapy, have enhanced the natural course of aHUS through hematologic remission induction, kidney function stabilization or improvement, and graft failure prevention. Since complement inhibitors are still unavailable in Egypt, it is important to understand the aHUS manifestations of pediatrics and adults in Egyptian hospitals, aiming for early diagnosis and proper management. In this study, we primarily aim to describe the aHUS burden on the patients by gathering their demographic and clinical characteristics, documented disease course, and long-term complications. Our secondary objectives include an estimate of the prevalence of patients diagnosed with aHUS out of all patients with TMA and gathering information about the clinical outcomes of available therapies in real-world settings, as there is no data from the country on aHUS management.

CONDITIONS

Official Title

The Burden of Atypical Hemolytic Uremic Syndrome and The Clinical Characteristics of Patients in Egyptian Hospitals A Multicenter, Observational, Retrospective Cohort Study in Egypt

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female patients aged one month or older who have been diagnosed with TMA between 01-Jan-2010 and 31-Dec-2023.
Not Eligible

You will not qualify if you...

  • None. All records of patients with TMA will be screened for aHUS diagnosis.

AI-Screening

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Trial Site Locations

Total: 8 locations

1

Research Site

Al Mansurah, Egypt

Not Yet Recruiting

2

Research Site

Alexandria, Egypt

Actively Recruiting

3

Research Site

Asyut, Egypt

Actively Recruiting

4

Research Site

Cairo, Egypt

Actively Recruiting

5

Research Site

New Cairo, Egypt

Not Yet Recruiting

6

Research Site

New Cairo, Egypt

Actively Recruiting

7

Research Site

Tanta, Egypt

Actively Recruiting

8

Research Site

Zagazig, Egypt

Actively Recruiting

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Research Team

A

AstraZeneca Clinical Study Information Center

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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The Burden of Atypical Hemolytic Uremic Syndrome and The Clinical Characteristics of Patients in Egyptian Hospitals A Multicenter, Observational, Retrospective Cohort Study in Egypt | DecenTrialz