How Can We Help You?
Find answers to common questions about our platform, clinical trials, and how we can help you.
A clinical trial is a research study involving people to test new treatments, drugs, or medical devices to see if they are safe and effective.
Clinical trials help discover new ways to prevent, detect, or treat diseases, improving healthcare and patient outcomes.
Anyone can participate in a clinical trial if they meet the specific eligibility criteria for that study.
Eligibility criteria are specific requirements such as age, gender, medical history, and current health condition that determine who can join a clinical trial.
Clinical trials typically have four phases, each testing the safety, effectiveness, and side effects of a treatment on different numbers of people.
Observational trials study health outcomes without changing how participants are treated. Interventional trials involve actively testing a treatment or intervention.
Clinical trials are sponsored by pharmaceutical companies, academic institutions, government agencies, or healthcare organizations.
Types include treatment, prevention, diagnostic, screening, and quality-of-life trials.
Clinical trials are carefully structured to answer research questions and include safety protocols to protect participants.
You can use MyTrials.ai to find clinical trials that match your medical profile based on your survey responses.
Consider factors like the potential benefits, risks, and the procedures involved.
Ask about the trial’s purpose, duration, risks, benefits, and your responsibilities during the study.
Benefits may include access to new treatments and compensation, while risks may involve side effects or ineffective treatment.
You may receive a specific treatment, undergo testing, and have regular health monitoring.
Yes, you can withdraw from a clinical trial at any time without penalty.
Most trials cover treatment and care. Some also cover travel and personal expenses.
You have the right to informed consent, privacy, safety, and to withdraw at any time.
Usually not, due to safety and data integrity concerns.
Our system uses an AI worker that can access any clinical trial in the world to help match patients. First, it pulls information from a central clinical trial database to create a personalized survey. After the patient completes the survey, our matching AI reviews all available trials and filters them based on each trial’s eligibility criteria—like age, condition, or medical history—to find the best matches. These probable matches are then presented to you!
MyTrials.ai uses AI-powered pre-screening to match patients with trials based on real-time eligibility criteria, reducing time spent on manual outreach and increasing overall enrollment efficiency.
By leveraging AI and dynamic surveys, we identify and qualify patients faster than traditional methods. Our platform shortens the recruitment funnel and minimizes screen failures by only connecting high-intent, eligible participants.
Yes, MyTrials.ai is designed to scale with multi-site and international trials. We provide region-based matching and localized pre-screening while maintaining a centralized dashboard for easy trial management.
We offer real-time dashboards with insights into referral volume, patient demographics, drop-off points, and engagement rates—empowering your team to optimize recruitment strategies as you go.
Yes. MyTrials.ai is built with data security and compliance in mind, adhering to standards like HIPAA, PIPEDA, and GDPR. We work closely with REBs/IRBs and follow best practices in informed consent and privacy protocols.
Reach out through our Contact page or schedule a demo with our team. We'll assess your trial needs, onboard your protocol, and start matching patients in as little as a few days.