FAQ
Frequently Asked Questions
Answers to common questions about clinical trials and Corterve.
General
A clinical trial is a research study that tests new medical approaches in people. These studies explore new methods of screening, prevention, diagnosis, or treatment. Every trial is reviewed and monitored by experts to ensure safety and scientific validity.
Yes. Corterve is completely free for patients — there are no hidden fees or costs. Enterprise pricing for sponsors and research sites is scoped to each engagement. Request a custom quote for organizational pricing.
We show trials that may relate to a person’s health profile and location. Final eligibility is always determined by the research team during their own screening process. We do not determine eligibility.
Corterve provides comprehensive community engagement support for research sites and sponsors. Contact us to discuss your specific needs and protocols.
Eligibility & Participation
Each trial has specific eligibility criteria. Our assessment helps identify trials where you may qualify, but final eligibility is always determined by the research team during their screening process.
Many clinical trials offer compensation for time and travel. The amount varies by study. Compensation details are provided when you review relevant trials.
Yes. Participation in any clinical trial is completely voluntary. You can withdraw at any time, for any reason, without penalty.
Privacy & Safety
Yes. We are HIPAA-aligned and use end-to-end encryption to protect your data. We never sell your personal information, and data is shared with research sites only when you explicitly consent.
Clinical trials are carefully designed and monitored. Every trial undergoes review by ethics committees (IRBs) before it begins, and participant safety is continuously monitored throughout.
Research teams closely monitor all participants. If you experience any adverse effects, report them immediately to the research team. Medical care for trial-related issues is typically provided at no cost.
Getting Started
The assessment typically takes 5–10 minutes. Questions focus on your health conditions, symptoms, and preferences.
You'll see trials that may fit your profile. You can review each trial and express interest — we'll then connect you with the research site to begin their screening process.
Yes, you can help a family member complete the assessment. All final decisions about participation must be made by the patient (or their legal guardian for minors).
Still Have Questions?
Tell us what you are working on and the right person will reply.
Book an Exploratory Call