GMMG Multiple Myeloma Registry
This study, called the GMMG Multiple Myeloma Registry, is designed to keep track of the long-term health of people in Germany with multiple myeloma. These individuals have previously participated in treatment studies run by a group called the German-Speaking Myeloma Multicenter Group (GMMG). The main goal is to collect information on how patients do over many years, looking at things like how long they live, how long they stay free from their cancer getting worse, and how their treatment plans change over time. By combining this new information with data from previous studies, researchers hope to get a clearer picture of the best ways to treat multiple myeloma and improve patients' lives. This is an 'observational' study, meaning patients receive their usual care, and researchers simply gather information without giving new treatments as part of this specific registry.
نظرة سريعة
ما هو موضوع هذه الدراسة؟
This registry is a long-term study that collects important health information from people in Germany who have multiple myeloma. Multiple myeloma is a type of cancer that affects plasma cells in the bone marrow. The people included in this registry have already taken part in previous treatment studies led by a group called the German-Speaking Myeloma Multicenter Group (GMMG).
The main idea behind this registry is to continue gathering information about these patients over many years, even after their original treatment studies have finished. This helps doctors and researchers understand the long-term effects of different treatments. They want to see how long people live overall, how long they stay well without their cancer getting worse, and what happens to their health over a long period. By combining this new, ongoing information with what they already know from the previous studies, they can learn a great deal about the best ways to manage multiple myeloma.
This kind of study is really important because it helps improve future care for others with multiple myeloma. It provides valuable insights into how treatments work in the real world and over time, allowing doctors to make more informed decisions and develop better treatment strategies. It started in late 2022 and involves many cancer centers across Germany.
النقاط الرئيسية
- This is a registry for people with multiple myeloma who were in past GMMG studies.
- It collects long-term health information to understand treatment effects over many years.
- No new treatments are given; you'll receive your usual care.
- Information is collected every 6-12 months.
- Your participation helps improve future care for multiple myeloma patients.
- You can withdraw from the registry at any time.
من قد يكون مؤهلاً؟
To be part of this registry, you must have previously participated in a treatment study run by the German-Speaking Myeloma Multicenter Group (GMMG). This means you would have already been treated for multiple myeloma as part of one of their specific research trials.
People who had a condition called organ amyloidosis at the time they were diagnosed with multiple myeloma would not be able to join this registry. Organ amyloidosis is when abnormal proteins build up in organs and can cause health problems.
This registry is open to adults aged 18 and older, and it includes both men and women.
هل يمكن أن تناسبك هذه الدراسة؟
أجب عن هذه الأسئلة السريعة لترى ما إذا كنت مؤهلاً. هذا دليل فقط - الفريق البحثي هو الذي يتخذ القرار النهائي.
- هل تم تشخيصي بالورم النخاعي المتعدد؟
- Did I previously take part in a treatment study from the GMMG group?
- Am I aged 18 or older?
- Did I NOT have organ amyloidosis when I was first diagnosed with multiple myeloma?
ماذا يتضمن المشاركة؟
If you are eligible and agree to take part, your contribution to this registry will mainly involve allowing researchers to continue gathering information about your health. You will continue to receive your standard medical care from your own doctors, as you normally would. This study does not involve new treatments or medical procedures.
Researchers will collect information every six months until your cancer progresses (gets worse). After that, they will collect information once a year. This data includes details about your treatment, your current health, and how you are doing. The information collected will be kept private and stored in a secure electronic system. You can choose to stop participating at any time.
المخاطر والفوائد المحتملة
المواقع (35)
- مستشفى هيليوس، عيادة أمراض الدم والأورام والمناعةالرمز البريدي المؤكدبرلين، ألمانيا· التوظيف
- Charité Campus Benjamin Franklin, III. Med. Abt. (Hämatologie/Onkologie)الرمز البريدي المؤكدبرلين، ألمانيا· التوظيف
- مستشفى بيليفيلد، عيادة أمراض الدم والأورام والطب التلطيفيالرمز البريدي المؤكدبيليفيلد، ألمانيا· التوظيف
- العيادة الطبية الجامعية، مستشفى كنابشافتالرمز البريدي المؤكدبوخوم، ألمانيا· التوظيف
- مستشفى جامعة بون، العيادة الطبية والعيادة الخارجية الثالثة، تخصص الأورام وأمراض الدم والروماتيزمالرمز البريدي المؤكدبون، ألمانيا· التوظيف
- Klinikum Chemnitz GmbH, Innere Medizin IIIالرمز البريدي المؤكدكيمنتس، ألمانيا· التوظيف
- Universitätsklinikum Köln, Klinik I - Innere Medizinالرمز البريدي المؤكدكولونيا، ألمانيا· التوظيف
- Onkologisches Studienzentrum Darmstadtالرمز البريدي المؤكددارمشتات، ألمانيا· التوظيف
- Klinikum Darmstadt, Med. Klinik V, Hämatologie/Onkologieالرمز البريدي المؤكددارمشتات، ألمانيا· التوظيف
- Universitätsklinikum Düsseldorf, Klinik für Hämatologie,Onkologie und Klin. Immunologieالرمز البريدي المؤكددوسلدورف، ألمانيا· التوظيف
- Universitätsklinik Erlangenالرمز البريدي المؤكدإرلانجن، ألمانيا· التوظيف
- Universitätsklinikum Essen, Klinik für Hämatologie und Stammzelltransplantationالرمز البريدي المؤكدإيسن، ألمانيا· التوظيف
أسئلة شائعة
What is the main goal of this registry?
The main goal is to collect long-term health information from people with multiple myeloma who were in previous GMMG treatment studies, to understand how treatments affect them over time.
Will I receive new treatment as part of this study?
No, this is an observational study. You will continue to receive your standard medical care from your own doctors, and no new treatments are given as part of this registry.
How often will my information be collected?
Your health information will be collected every six months until your cancer progresses, and then once a year after that.
ما نوع المعلومات التي سيتم جمعها؟
Researchers will collect details about your treatments, how your health is doing, and important milestones like how long you stay well or if your condition changes.
هل يمكنني التوقف عن المشاركة إذا غيرت رأيي؟
Yes, you can choose to stop participating in the registry at any time, and this will not affect the medical care you receive.
كيفية معرفة المزيد
Eileen Kurre
تحدث دائمًا إلى طبيبك العام أو الأخصائي قبل اتخاذ قرار بالمشاركة في دراسة.
هل أنت مهتم بالمشاركة؟
نقاش
مناقشة المجتمع
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