Our clinical studies offer new paths to understanding and treating multiple chronic health conditions, aiming to shape future care standards.
At Rhyk, we believe every medical breakthrough must be proven with a clinical study. These critical research studies are fundamental of medical innovation, determining the safety and efficacy of new treatments for various of conditions. By participating in a Rhyk clinical study, you're not just gaining access to potential new treatments - you're also contributing to valuable medical research that can benefit countless others in the future. Whether you're a medical professional interested in collaborating, or you’re a patient seeking new treatment options, your participation is an important part of developing the next generation of medical therapies.
Participants receive trial medication and related care at no cost, providing an opportunity to explore new medical options.
Your involvement directly supports the development of safe and effective treatments, potentially improving the lives of people around the world.
Interested in learning more or participating in a study? Fill out our contact form to connect with us. Specify your interest area to help us provide you with the most relevant information.
A clinical study is a structured research initiative with human participants to assess the effectiveness and safety of innovative treatment methods, such as biostimulation technologies. The goal is to answer specific questions about new therapeutic approaches or enhancements to existing treatments, focusing on their impact on human health. For example: “Does this treatment work?”, “Does it work better than other options?” and many more. Rhyk’s commitment to advancing healthcare solutions involves conducting clinical studies to directly evaluate how new treatments perform in real-world settings, ensuring they are both effective and safe for patient use.
Clinical studies are important for verifying that innovative treatments meet high standards of patient safety and provide significant health benefits. By systematically gathering data on treatment outcomes, efficacy, and participant experiences, our clinical studies aim to improve therapeutic patient care and contribute to the broader field of medical science.
No, participants do not have to pay to take part in our clinical trials. Rhyk covers all medical expenses that are directly related to the study, including treatments, examinations, and any specific procedures required by the study protocol. Our priority is to ensure that financial concerns do not prevent anyone from accessing potentially beneficial treatments and contributing to medical advancements.
Participants in our clinical studies do not receive financial compensation. Participants are qualified as suitable candidates by their clinics or healthcare providers and agree to participate in the study primarily for the potential personal health benefits. Our participants are motivated by the opportunity to access new treatments and by the possibility of contributing to research that may benefit countless other patients in the future. We deeply appreciate the commitment and contribution of all participants, and are grateful for their contribution to the progress of medical science.
Eligibility for participation in our clinical studies is determined by the doctors at the clinics and points of care we collaborate with. These clinical partners select participants from their existing patient pools based on specific criteria, such as age, type and stage of a condition, medical history, and current health status. This targeted approach ensures the safety of participants and maintains the integrity of the study results. If you are interested in participating in a clinical study and believe you might be eligible, we recommend discussing this with your healthcare provider. They can contact us directly and provide information on any current or upcoming studies that may be suitable for you, based on your health condition and medical history.
Participating in a clinical study comes with both potential benefits, such as gaining access to new treatments before they are widely available, and potential risks, which rarely may include experiencing unknown side effects. All known risks and benefits will be thoroughly explained during the Informed Consent Process before you decide to participate.
The duration of a clinical study can depend on the study’s set-up, the type of treatment being studied, and the specific study requirements. Participants are informed about the estimated timeline before singing up, and any changes to the trial duration will be communicated immediately.
Protecting the privacy and confidentiality of our participants is important to us. All personal information is handled in accordance with strict data protection regulations. Information collected during the study is used exclusively for research purposes and any publication of the results will be done in a way that ensures participants cannot be individually identified.
Rhyk Technologies GmbH
Bundeskanzlerplatz 2d
53113 Bonn
Stollbergstraße 22
80539 München
© Copyright 2024 – Rhyk Technologies GmbH. All Rights Reserved.
© Copyright 2024 – Rhyk Technologies GmbH. All Rights Reserved.
