Know if your site can enroll. Before you commit.
Clinical Enroll's AI feasibility tool analyzes your protocol against local patient population data, competing trial activity, and digital channel viability. You get a full enrollment report in 24 hours.
Six analyses. One document. 24 hours.
Most sites answer feasibility questionnaires from memory or from a single prior campaign. The Clinical Enroll report gives you protocol-specific data sourced from patient population estimates, ClinicalTrials.gov, and digital channel benchmarks.
Patient Enrollment Funnel
Projected path from ad response to randomization. Leads generated, protocol-screened patients, and enrolled patients modeled from your protocol's criteria and local population data.
Estimated Cost Per Randomized Patient
Budget range based on your protocol's leads-to-randomization ratio and CPL benchmarks for your indication. Know your expected cost before you commit.
Competitive Landscape
Are other trials actively recruiting for the same patients within 50 miles of your site? We check every active competing study and tell you whether your patient pool is contested or exclusive.
Digital Outreach Potential
Channel-by-channel scoring for Meta and Google Ads. We assess reach, audience targetability, and estimated CPL for your specific indication and site geography.
Protocol Risk Assessment
What works in your favor and what works against you, specific to your eligibility criteria, patient population, and site geography. Plus what it all means for your enrollment timeline.
Recommended Campaign Approach
The specific creative strategy, pre-screening questionnaire design, and channel mix Clinical Enroll would build for this study. Actionable whether you run the campaign with us or not.
A sample of what you receive.
Each report is generated for your specific NCT number, site location, and enrollment target. Below is an excerpt from an Eosinophilic Asthma Phase 3 analysis.
Executive Summary
Recruitment
Outlook
Sponsor
Your Sponsor
Phase
Phase 2/3
Enrollment Target
Your Target
US Sites
Active
Digital Outreach
8/10
Meta + Google
Difficulty
Moderate
Eligibility complexity
Enrollment Analysis
The Patient Enrollment Funnel
1 in 35
ad responses converts to an enrolled patient
1 in 3
leads qualify for screening
8%
screened go on to randomize
Competitive Landscape
Competing Trial Activity in Your Geography
100%
Uncontested patient pool
No other site is recruiting for the same eligible patients in your market.
~25%
Est. CPL reduction vs. contested markets
0
Competing studies seen by patients here
Exclusive recruitment territory
Budget Intelligence
Estimated Cost Per Randomized Patient
$6,300–$11,200
Estimated cost per randomized patient
At $180–$320 CPL, the 35:1 lead ratio implies this range per randomized patient.
Patient Population
~25M addressable
Leads That Qualify
13%
Built for site-side professionals.
Site Directors
A sponsor asks if your site can enroll 10 patients by Q3. The report tells you if it's actually achievable — and what it would cost.
Study Coordinators
You're completing a sponsor feasibility questionnaire. The report gives you enrollment funnel data and realistic timeline estimates to fill it accurately.
Principal Investigators
You're evaluating whether to take on a protocol. The competitive landscape and patient population data tell you what you're walking into before you commit.
From NCT number to full report in 24 hours.
01
Submit your NCT number
Paste your study's ClinicalTrials.gov identifier. Submit up to 3 studies at once during early access. No call required.
02
We run the analysis
Our AI cross-references your protocol's criteria against patient population data, active competing trials, and digital channel reach for your site geography.
03
You receive the full report
Within 24 hours. Web report plus PDF download. Enrollment funnel, cost estimates, competitive landscape, channel scoring, and a recommended campaign approach.
Submit up to 3 studies. Get all three free.
During early access, Clinical Enroll is generating enrollment feasibility reports at no cost for qualifying research sites. Submit your NCT numbers and receive your full reports within 24 hours.
Up to 3
Studies per submission
Within 24 hours
Delivery
Free
Cost
PDF + web report
Format
GHL Early Access Form
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Early access is available to clinical research sites in the United States. Reports are generated using ClinicalTrials.gov data, U.S. Census population estimates, and Clinical Enroll's channel benchmarks.
Already working with Clinical Enroll? Submit an NCT number for a full feasibility evaluation and campaign proposal.