Non-interventional Study of Patients With Transthyretin (ATTR) Amyloidosis
The MaesTTRo study is a worldwide study for people with a condition called transthyretin amyloidosis (ATTR). It’s not testing a new treatment, but rather observing how patients live with ATTR and how their current treatments are working over several years. This includes conditions like ATTR affecting the heart (ATTR-CM) or nerves (ATTRv-PN). The study will collect information from patients during their regular clinic visits about their health and the effects of their treatments. This helps doctors better understand the disease and improve care in the future. Data will be collected securely, with patient privacy as a top priority.
Auf einen Blick
Worum geht es in dieser Studie?
Imagine a condition where certain proteins build up in your body, affecting parts like your heart or nerves. This is what happens in transthyretin amyloidosis (ATTR). The MaesTTRo study is an important non-interventional study, which means it’s not testing a new drug or procedure. Instead, it’s like watching a long-running movie about people with ATTR from all over the world.
The main goal is to understand how ATTR naturally progresses over time and how different treatments are being used in regular care. Researchers want to see what really happens in daily life for people with this condition and how well existing treatments, including newer ones like eplontersen, are actually working. This information is incredibly valuable because it helps doctors and researchers improve care for future patients.
By gathering information from many patients, the study will provide a clearer picture of ATTR and its treatments. It helps us learn more about symptoms, how the disease changes, and the true impact of different treatments in a real-world setting, rather than in a highly controlled trial. This knowledge can lead to better ways to manage the condition and support people living with ATTR.
Wichtige Erkenntnisse
- It's an observational study, not testing new drugs.
- Aims to understand ATTR and real-world treatment use.
- No extra clinic visits or procedures are needed.
- You'll complete questionnaires during routine appointments.
- Participation lasts 3 to 7 years.
- Your contribution helps future understanding of ATTR.
Wer könnte berechtigt sein?
To take part in the MaesTTRo study, you would need to be at least 18 years old and have a confirmed diagnosis of transthyretin amyloidosis (ATTR). It's also important that you are willing and able to understand and sign a consent form, and fill out some health questionnaires on a regular basis.
There are some reasons why you wouldn't be able to join. For example, if you are currently taking part in another clinical trial that is testing a new treatment for ATTR. Also, if you have other types of amyloidosis, like AL or AA amyloidosis, or if you have ATTR but do not have any symptoms yet, you wouldn't be eligible for this particular study.
Könnte diese Studie für Sie geeignet sein?
Beantworten Sie diese kurzen Fragen, um zu sehen, ob Sie möglicherweise berechtigt sind. Dies ist nur ein Leitfaden – das Forschungsteam trifft die endgültige Entscheidung.
- Sind Sie 18 Jahre alt oder älter?
- Do you have a confirmed diagnosis of ATTR amyloidosis?
- Are you willing to complete online health questionnaires?
- Are you NOT currently in another ATTR treatment trial?
- Do you NOT have AL or AA amyloidosis?
- Do you have ATTR symptoms?
Was beinhaltet die Teilnahme?
If you decide to join the MaesTTRo study, you won't need any extra clinic visits or procedures. All the information will be collected during your usual appointments with your doctor. You'll be asked to fill out some electronic health questionnaires about your well-being when you first join and then every six months during your routine clinic visits. These questionnaires help researchers understand how you're feeling and how your condition affects you.
The study will also gather information about your health and treatments from your medical records, just as your doctor usually collects it. There are no new medications to take as part of this study. The total time you'd be involved in the study could range from at least three years, up to seven years, depending on when you join.
Potenzielle Risiken und Vorteile
Locations (89)
- ForschungsseiteVerifizierte PostleitzahlLa Jolla, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlLos Angeles, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlSan Francisco, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlSan Francisco, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlNew Haven, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlWashington D.C., Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlChicago, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlIndianapolis, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlBaltimore, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlBoston, Vereinigte Staaten· Rekrutierung
- ForschungsseiteVerifizierte PostleitzahlBoston, Vereinigte Staaten· Noch nicht rekrutiert
- ForschungsseiteVerifizierte PostleitzahlBoston, Vereinigte Staaten· Rekrutierung
Häufige Fragen
What is the main purpose of the MaesTTRo study?
It's observing people with ATTR over time to understand the condition and how real-world treatments are working.
Do I need to take new medication for this study?
No, this study doesn't involve any new medications. It observes the treatments you are already receiving.
Wie lange werde ich an der Studie teilnehmen?
You'll be followed for at least three years, and potentially up to seven years depending on when you join.
Werde ich zusätzliche Arzttermine haben?
No, all study information will be collected during your regular, routine clinic visits.
How will my personal information be kept safe?
Your privacy is important. In some regions like the US, personal details might be replaced with secure codes, and only anonymous information will be used for analysis.
Wie Sie mehr erfahren können
AstraZeneca Klinisches Studieninformationszentrum
Sprechen Sie immer mit Ihrem Hausarzt oder Spezialisten, bevor Sie sich entscheiden, an einer Studie teilzunehmen.
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