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Atypical Hemolytic-Uremic Syndrome (aHUS) Registry

This study, called the Atypical Hemolytic-Uremic Syndrome (aHUS) Registry, is designed to collect important safety information after new medicines like eculizumab and ravulizumab have been approved and are being used by patients. It helps doctors understand how safe these treatments are in real-world use. The study also tracks how aHUS affects patients over time, regardless of whether they are on these specific treatments or not. It's open to people of all ages, including children, who have been diagnosed with aHUS. The main goal is to improve our understanding of aHUS and its treatments to help future patients.

A colpo d'occhio

Stato
Reclutamento
Sponsor
Alexion Pharmaceuticals, Inc.
Obiettivo di iscrizione
3,000
Inizio
18 Mar 2013
Completamento stimato
01 Gen 2031

Di cosa tratta questo studio?

This registry is a study for people with a rare kidney condition called atypical Hemolytic-Uremic Syndrome, or aHUS. When new medicines are approved, doctors need to keep learning how they work in real life. This study collects information on patients who are treated with two specific medicines, eculizumab or ravulizumab, to see how safe they are once they've been approved and are being used widely. This is called 'post-marketing safety data'.

But it's not just about these medicines. The study also collects details on how aHUS affects patients over time, no matter what treatment they are receiving, or even if they aren't on these particular medicines. This helps doctors and researchers understand the condition better and how it progresses in different people.

By gathering this information from many patients, researchers hope to get a clearer picture of aHUS and how best to manage it. This can lead to better care and understanding for everyone affected by this rare disease in the future.

Punti chiave

  • It's a study about a rare kidney disease called aHUS.
  • It collects information on how aHUS progresses and how safe certain medicines are.
  • Participation involves sharing medical information, not new treatments.
  • It's open to patients of all ages, including children.
  • The goal is to improve understanding and care for aHUS patients.

Chi può essere idoneo?

You might be able to join this study if you've been diagnosed with atypical Hemolytic-Uremic Syndrome (aHUS). This includes people of all ages, from young children to adults. It doesn't matter if doctors have found a specific genetic cause for your aHUS or not.

An important part of joining is being able to understand and sign a consent form. If you're under 18, your parent or legal guardian would sign for you, and you would also be asked if you're happy to take part.

You would not be able to join if your Hemolytic Uremic Syndrome (HUS) is only caused by a specific type of E. coli bacteria (Shiga Toxin producing E. coli). Also, if you or your guardian are unable to give written consent, then you would not be able to take part.

Questo studio potrebbe fare al caso tuo?

Rispondi a queste domande rapide per vedere se potresti essere idoneo. Questo è solo una guida — il team di ricerca prende la decisione finale.

  1. I have been diagnosed with atypical Hemolytic-Uremic Syndrome (aHUS).
  2. My HUS is not caused only by a specific E. coli infection.
  3. I (or my parent/guardian if I'm under 18) can understand and give written permission to take part.
  4. If I'm under 18, I am happy to take part myself.
Rispondi a ogni domanda per vedere il tuo risultato.

Cosa comporta la partecipazione?

This study is a registry, which means it mainly involves collecting information about your condition and treatment from your medical records. You would continue to receive your usual medical care from your own doctors. There are no specific study visits or extra medication given as part of this registry. Your treatment decisions would be made by you and your doctor as normal. The study would gather information over a period of time, tracking your health and any treatments you receive for aHUS.

Rischi e benefici potenziali

Taking part in this study may not directly benefit you, but the information collected will help doctors and researchers better understand aHUS and its treatments for future patients. This could lead to improved care for others. There are very few direct risks to participating, as it primarily involves collecting information from your medical records. Your medical care would not change. You are always free to decide to stop participating in the study at any time without it affecting your medical care.

Locations (141)

  • Clinical Trial Site
    Codice postale verificato
    Aurora, Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Washington D.C., Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Gainesville, Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Atlanta, Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Chicago, Stati Uniti· Ritirato
  • Clinical Trial Site
    Codice postale verificato
    Boston, Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    St Louis, Stati Uniti· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Winston-Salem, Stati Uniti· Ritirato
  • Clinical Trial Site
    Codice postale verificato
    Columbus, Stati Uniti· Attivo ma non reclutante
  • Clinical Trial Site 1
    Codice postale verificato
    Westmead, Australia· Reclutamento
  • Clinical Trial Site 2
    Codice postale verificato
    Westmead, Australia· Reclutamento
  • Clinical Trial Site
    Codice postale verificato
    Cairns, Australia· Reclutamento

Domande comuni

What is atypical Hemolytic-Uremic Syndrome (aHUS)?

It's a very rare and serious kidney disease that can damage blood vessels.

Will I get new medicine in this study?

No, this study only collects information about your current medical care and treatments.

Chi può partecipare a questo studio?

People of all ages diagnosed with aHUS, as long as it's not caused by a specific E. coli infection.

What information will the study collect?

It will gather details about your aHUS, its progression, and any treatments you receive.

Posso abbandonare lo studio se cambio idea?

Yes, you can withdraw from the study at any time without affecting your medical care.

Come saperne di più

Alexion Pharmaceuticals, Inc. (Sponsor)

Parla sempre con il tuo medico di base o specialista prima di decidere di partecipare a uno studio.

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