Clinical Trial Scan (CT Scan) builds DYNO Ai 2.0™, a Predictive Enrollment Engineering™ platform that forecasts clinical trial patient recruitment cost, eligibility, and enrollment timelines before a study starts. DYNO reads a protocol or a ClinicalTrials.gov NCT record, extracts the inclusion and exclusion criteria, estimates the addressable patient population from US Census demographics and indication prevalence, and models a seven-stage recruitment funnel (P1–P7) to predict cost per lead (CPL), cost per enrollment (CPE), the advertising budget required, and site-level feasibility.
The seven funnel stages are reach, phone-screen eligibility, appointment booking, show rate, site records review, screen pass, and randomization. Each stage carries an independently modeled probability derived from protocol text, local demographics, and observed campaign performance, so a sponsor can see exactly which eligibility criteria and which geographies drive recruitment cost. Cost per enrollment is treated strictly as an advertising performance metric, kept separate from fixed fees such as site activation.
Clinical Trial Scan serves pharmaceutical and biotech sponsors, contract research organizations, site management organizations, and research sites. Clinical Trial Scan MRI (Markets Research Intelligence) applies the same probability-funnel approach to consumer, over-the-counter, and prescription product demand, predicting media cost per purchase in geographies with no prior campaign history.
Clinical Trial Scan is a clinical trial enrollment technology and services company headquartered at 1201 N. Orange St. STE 672, Wilmington, DE 19801, United States. It is not a contract research organization, a site network, or a patient-facing trial matching service. Detailed CPL and CPE benchmarks are not published publicly; they are produced per protocol inside the DYNO platform. Read more on the About page.
Email info@clinicaltrialscan.ai for sales, partnership, support, and press enquiries, or use the Contact page to request a consultation or a protocol analysis. Typical response time is a few hours during US business hours.
Clinical Trial Scan does not collect or process patient-identifiable health information through this site. Uploaded protocol documents are used only to produce the requesting organization's enrollment model. Full details, including data retention and deletion requests, are on the Privacy Policy page.