Patients Participating in Research – the Good, Bad and Ugly!
Clinical Drug Trials refer to the scientific study...
Welcome to our FAQ page! We’ve compiled a list of commonly asked questions to help you find answers quickly. If you can’t find what you’re looking for, feel free to contact our support team.
Clinical research refers to scientific studies conducted on humans to evaluate the safety, effectiveness, and benefits of new medical treatments, medications, therapies, or devices.
You can participate in clinical research studies by searching for ongoing trials on our website and applying to participate in a study that matches your eligibility criteria.
Yes, clinical research studies are designed with strict ethical guidelines and safety measures to ensure the well-being of participants. All studies are reviewed and approved by regulatory bodies before they can begin.
The duration of a clinical research study can vary depending on the nature of the study and the treatment being evaluated. Some studies may last for a few weeks, while others can span several years.
By participating in a clinical research study, you may gain access to cutting-edge treatments or medications that are not yet widely available. Additionally, you contribute to advancing medical knowledge and helping future patients.
While measures are taken to minimize risks, some studies may have potential risks or side effects. It is important to carefully review all the information provided by the study team before deciding to participate.
Some clinical research studies may offer compensation to participants for their time, travel expenses, or other inconveniences. The study details will specify if compensation is available.
Participants in clinical research studies are protected by informed consent, privacy regulations, and ethical guidelines. These ensure that participants are fully aware of the study's purpose, potential risks, and benefits before making a decision to participate.
Yes, participants have the right to withdraw from a clinical research study at any time without penalty. You should communicate your decision to the study team, who will provide guidance on how to safely exit the study.
Clinical research studies are regulated by government agencies, such as the Food and Drug Administration (FDA), and ethical review boards. These regulatory bodies ensure that studies comply with safety regulations and ethical standards.
Eligibility criteria for each study vary, and some studies may specifically focus on patients with certain medical conditions. However, there are often studies available for individuals with pre-existing conditions, so it is worth exploring the options.
Once a clinical research study is complete, the results are carefully analyzed by the study team and, if applicable, submitted for publication in medical journals. The findings may inform future treatments or practices.
Participating in multiple clinical research studies simultaneously may not be possible due to potential interactions or conflicts between study protocols. It is best to check with the study team about their specific requirements.
Clinical research studies can be funded by pharmaceutical companies, government agencies, academic institutions, or non-profit organizations dedicated to advancing medical knowledge and patient care.
In some cases, the study team may need to remove a participant if their health deteriorates or if unforeseen risks emerge. This is done to prioritize participant safety and minimize any potential harm.
Age restrictions can vary depending on the study. Some studies may have specific age requirements, while others may be open to individuals of all ages. Eligibility criteria are detailed in the study descriptions.
Yes, your medical information will be kept strictly confidential during a clinical research study. Data protection laws and ethical guidelines ensure that participant information is securely handled and anonymized.
Before participating, you should carefully review the study details, including the potential risks, benefits, time commitment, and any specific requirements. Discuss the decision with your healthcare provider or the study team to make an informed choice.
Pregnancy and breastfeeding can be exclusion criteria for some studies due to potential risks to the fetus or infant. However, there may be studies specifically designed for pregnant or breastfeeding individuals. Check the study eligibility criteria for more information.
You can stay informed about new clinical research studies by subscribing to our newsletter or following our website and social media channels. We regularly update our platforms with new study opportunities for interested individuals.
SYNCRETIC has always given importance to quality, integrity and adherence to promised timelines. Contact us to know more about our services.
Clinical Drug Trials refer to the scientific study...
Clinical research designs have always been a topic...
So, what exactly does it mean when we...
What is Clinical Research and Why Is it Important? Clinical...
Syncretic offers you a one-stop solution for all your clinical research needs. Get in touch to know more.
A small step in clinical research can become a giant leap in global healthcare.