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Krijg vandaag toegang tot de behandelingen van morgen.

Vind één van de 24.723 klinische onderzoeken die zijn gevalideerd door het Europees Geneesmiddelenagentschap waarvoor men momenteel kandidaten zoekt.

Eenvoudig als 1, 2, 3

1. Maak uw veilig profiel aan

Beantwoord de vragen van onze AI op basis van de duizenden onderzoeken die momenteel gaande zijn.

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2. Een lijst met onderzoeken ontvangen

Op basis van uw antwoorden zal Curewiki een lijst maken met onderzoeken die overeenkomen met uw profiel en voorkeuren.

3. Meld u aan (of niet)

U beslist of u zich als vrijwilliger wilt aanmelden en wordt in contact gebracht met de persoon die verantwoordelijk is voor het onderzoek.

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Zich aanmelden verplicht u tot niets meer dan het ontvangen van proefaanbiedingen.

Sluit u aan bij 26.000 vrijwilligers

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Bent u ziek?

Krijg toegang tot nieuwe behandelingen en help de geneeskunde.

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Bent u NIET ziek?

Onderzoekers hebben ook gezonde (betaalde) vrijwilligers nodig.

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Wilt u helpen?

Vertel het verder en help de Curewiki-beweging groeien!

“Iedereen heeft het recht om deel te nemen aan medisch onderzoek. Daarom bieden wij toegang tot alle klinische onderzoeken die in Europa worden gedaan, en onze onafhankelijkheid maximaliseert uw kansen om het juiste onderzoek voor uw behoeften te vinden.”

Jean-Sébastien, oprichter van Curewiki

Curewiki is een Europese start-up (12 mensen in Nederland, België en Spanje) opgericht in 2022 en gefinancierd door publieke en private fondsen.

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Jean-Sebastien Gosuin

Als kind overwon hij kanker. Nu wil hij dat iedereen toegang heeft tot de beste behandelingen. Hij leidt het bedrijf.

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Edwin Klumper

Als voormalig arts die geconfronteerd werd met de moeilijkheid om een onderzoek te vinden voor patiënten of bekenden, richtte hij een bedrijf voor medisch onderzoek op voordat hij bij Curewiki kwam. Hij is verantwoordelijk voor de Commerciële Relaties.

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Roel Divendael

Hij werkte 15 jaar in medisch onderzoek en wijdt nu zijn tijd aan patiënten en onderzoekers aan elkaar linken. Hij is verantwoordelijk voor Ondersteuning.

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Fabienne Bourel

Zoals iedereen heeft zij dierbaren verloren en zijn vele anderen ziek, maar ze vinden geen oplossing. Zij is verantwoordelijk voor Communicatie.

  • What is a Clinical Trial?
    The clinical trial is the final step in the development of a drug or treatment. Involving patients, healthy volunteers or both, a clinical trial is one part of a long and careful research process. A clinical trial explores whether a medical strategy, treatment or device is safe and effective for humans.
  • Why Clinical Trials are Important?
    Although all new drugs, treatments and devices are rigorously tested in the laboratory they must also go through clinical trials so more can be found out about their potential benefits or risks. Clinical trials provide researchers with the opportunity to potentially find better treatments for others in the future, as well as offering hope for many people
  • Why take part in clinical trials?
    - To have access to innovative treatments before they are available and accessible to other patients. - To have access to the care of specialist health professionals and their additional advice. - To receive compensation, financial reimbursement or health services. - To contribute to medical advances and the development of new treatments or therapies. - To help others suffering from health problems. Need more? Read our blog post "5 reasons to take part in a clinical study"
  • What are the benefits of being in a clinical trial?
    - You may be given a treatment which isn’t available elsewhere and that is safer or works better than current treatment options. - You could be helping others who may have the same condition in the future by advancing knowledge in that condition/disease - You may increase the total number of therapeutic options available to you - You may feel like you have more choice over your situation and are taking a more active role in your health - You could gain access to newer, more innovative treatments, the possibility of additional care/ attention and more careful monitoring of your condition by your healthcare team
  • What are the potential risks?
    - The new treatment may have unknown side effects or other risks, which may or may not be worse than those from existing treatments - The treatment may not work for you, even though it works for others - The treatment may not be as effective as current treatment options - The impact it may have on your lifestyle, such as more frequent doctor visits and more tests - You may not be given the study treatment, as some trials such as randomised clinical trials are designed in a way where you may not have a choice about which treatment you are given. If the trial is blinded, you (and maybe your doctor) will not be told which treatment you are getting
  • Who can participate in a clinical trial?
    Both as a healthy volunteer or as a patient you can apply to participate in a clinical trial. Applying is not in itself a guarantee that you will be included in the clinical trial because the selection depends on your profile.
  • What diseases are covered by Curewiki?
    Our Curewiki platform includes an extensive database of over 3,000 diseases, both common and rare. Our mission is to provide opportunities for as many users as possible to take part in clinical trials.
  • Do I get paid?
    Healthy volunteers can be paid. Patients usually receive the treatment for free and more intensive follow-up by medical staff. They are not allowed to be paid by law, but they may be reimbursed for travel and other expenses related to the trial.
  • Are there any clinical trials near me?
    Yes, thousands of clinical trials take place every year in your country. Register now
  • What to expect if you are enrolled in a clinical trial?
    If you take part in a clinical trial you will be monitored regularly during and after the trial. You may find your clinical trial involves you having a number of tests, appointments and some things which you may need to do at home. The tests that you will need to have will depend on the disease or condition that you have, and the trial you have entered.
  • What clinical trials are we looking for?
    We only list clinical trials validated by national and international drug agencies. Medical trials listed by national and international medical agencies typically adhere to rigorous ethical guidelines and regulatory standards. Participating in these trials ensures that you are involved in studies that prioritise participant safety, informed consent, and ethical conduct.
  • If I participate in a clinical trial, what are my rights?
    As a participant, you have the right : - to participate voluntarily, without pressure or repercussions if you elect not participate - to leave the trial at any time; - free treatment and, usually, free examinations as part of the clinical trial; - possible early access to new medicines; - a possible indemnity assessed by the ethics committees, to compensate for any costs incurred and time spent on medical research. The compensation is not determined according to the potential risk involved; - to receive all the information necessary to give your consent before any procedure; - to clear and understandable answers to your questions; - to be informed immediately, even after the start of the trial, if new data is collected that could influence your decision to participate; - safe care that respects your beliefs; - confidential and anonymous treatment of your data; - insurance coverage from the trial sponsor. (Source: afmps - agence fédérale des médicaments et des produits de santé)
  • If I participate in a clinical trial, what are my duties?
    As a participant, you agree to : - to provide truthful and complete information about your health and medical history and any treatment you have taken - to comply with the clinical trial protocol and to cooperate with the medical staff; - undergo additional visits and assessments, which may be intensive. (Source: afmps - agence fédérale des médicaments et des produits de santé)
  • What are the duties of the organisers of a clinical trial?
    The medical team of the research centre plays a very important role in supporting, monitoring and informing the participants. This role does not end when the trial is over. The investigating doctor must explain the different aspects of the trial in the most comprehensible and complete way possible. As a potential participant, you can decide to participate with all the information available. This decision is recorded in a document that you must sign as a participant in a clinical trial. This informed consent describes the course of the trial in an understandable way, as well as the course you will follow as a participant. This document also describes your rights and duties as a participant. The organiser of a clinical trial must also take out "no fault" insurance. This means that you, as a participant, are insured, even if the doctor is not at fault. (Source: afmps - agence fédérale des médicaments et des produits de santé)
  • Why my data are needed to find clinical trials?
    By sharing your medical data with Curewiki, you enable us to target the clinical trials best suited to your situation. To do this, we align your needs with the specific criteria of the studies. Our commitment: to secure your information with advanced encryption and guarantee its confidentiality. We will never share your data without your prior consent.

FAQ.

Hebt u vragen? Bekijk onze FAQ's hiernaast. We hebben vast al een antwoord voor u.

Ontdek het klinische onderzoek dat bij u past en kies of u zich wilt aanmelden.

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STOP NIET MET GELOVEN.

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