Clinical trial feasibility

Know who qualifies
before your trial starts.

Check your eligibility rules against real US health data. In minutes.

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Meet your US Population Twin

Move the sliders. See how many people share your profile.

…US adults match this profile

Counted from sex, age, BMI and smoking. Blood pressure only changes the risks.

Loading CDC NHANES data…

Educational simulation based on CDC NHANES 2015–2018. Not medical advice.

Top health risks

    See all 10 risks

    Validated on published research

    See it on real trials

    Pick a trial and watch its rules apply.

    Each square is 1% of the starting group. Squares fade as each eligibility rule removes people.

    1 square = 1% of 243.8 million US adults

    On all five trials the published number falls inside our range, within about 1 percentage point.

    37.4%91.2 million US adults qualify
    Trial Fit
    91.2 million
    Published
    93.0 million
    Published number is inside our range −0.7 pts

    Our range

    83.2 million – 99.2 million

    Published source

    Wong et al., Cardiovasc Drugs Ther 2023

    Rule by rule

    Of 243.8 million US adults, about 91.2 million (37.4%) meet every rule we can check. Biggest cut: Obesity (BMI 30+), or overweight (BMI 27+) with a weight-related health problem (removes 47% of the group).

    Same rules, using the standard medical cut-offs (for example blood pressure 140/90). This reproduces the numbers in the researchers' own flowchart.

    Same 243.8 million starting population. Paper rules as written give 42.2%; classic thresholds reproduce the paper's flowchart.

    1. No diabetes85.0%
    2. Obesity (BMI 30+), or overweight (BMI 27+) with a weight-related health problem38.4%
    3. No previous weight-loss surgery37.5%
    4. No kidney failure37.4%

    Source: Wong et al., Cardiovasc Drugs Ther 2023. Data: CDC NHANES 2015–2018. Shares are of US adults.

    See the full report

    Before you ask sites

    Tune the criteria first. Ask sites once.

    Manual feasibility asks specific sites how many patients they can recruit. It takes weeks and costs thousands.

    Trial Fit answers a different question in minutes: what share of US adults meet your criteria, and which rule cuts the most people.

    See the accuracy comparison

    Trial Fit

    Time
    Minutes
    Cost
    Free preview, $349 report
    Based on
    Examined people, CDC NHANES

    Manual feasibility

    Time
    Weeks
    Cost
    Thousands to tens of thousands
    Based on
    Estimates from sites

    Pricing

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    Free preview

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    The headline number for your trial

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    Questions

    The headline number for your trial is free. The full report — range, the rules that exclude the most people, which rule to relax, what can't be checked, assumptions and a PDF — is $349, one-time. Payments are in test mode during the preview.

    Ideally the full protocol. A ClinicalTrials.gov ID works too, but it usually lists only a summary of the criteria (STEP 1 shows a few; its protocol has 35), so the number is less precise.

    Files are read in your browser; only the text is sent to compute the report. We don't publish or share it.

    On the five trials with published reference numbers, Trial Fit is within about 1 percentage point of published reference numbers (absolute: e.g. 37.4% vs 38% for STEP 1), and all published numbers fall inside our range. For other trials there is no reference, so the report shows every assumption and what can't be checked. Try them on the home page.

    No. A feasibility study asks your sites how many patients they can recruit. Trial Fit comes before it: in minutes it shows what share of US adults meet your criteria and which criterion cuts the most people, so you can tune the protocol first and run site feasibility once, on the final version.

    The United States today (CDC NHANES). The UK, EU and others are next.

    No. AI only translates the wording into rules from a fixed list of survey questions; you review them, and the engine computes every number.

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