Everything Clin2 offers, in one place

Your study, in plain words

Every registry record rewritten for real people — what it’s testing, who it’s for, what taking part involves — so patients actually understand it.

Search the way patients talk

Patients search by condition, treatment, or location in their own words, with autocomplete and meaning-aware matching that surfaces the right studies.

A fit read before any contact

We map a study’s criteria to plain questions and give patients a fit read before they ever reach a site — fewer mismatched conversations for your team.

Landing pages that get found

Browsable, search-optimized pages for every condition and therapeutic area, putting recruiting studies in front of patients already looking.

Patients come back

Patients save studies and opt in to hear when a new one fits their profile — keeping your studies discoverable as they open.

Social proof, de-identified

Each study, condition, and specialty page shows real, de-identified view activity — momentum that builds patient trust.

See them as patients do

See the studies you sponsor or run the way patients do, alongside their performance. (Adding studies to your account yourself is a Pro feature.)

Add studies yourself

Add the studies you want to track by NCT id, right from your portal — no waiting on us. Your first study is included with Pro; each additional study is $49/mo, added to your subscription.

Every engagement, per study

Views, pre-screen starts, completions, and applications for each of your studies — the full engagement picture.

Momentum at a glance

Headline view counts across rolling windows, so you see movement — not just a lifetime total.

Spot a rise or a stall

A clean daily view trend for every study, so a change in interest is obvious immediately.

Where patients drop off

How far patients get through your pre-screen and where they fall away — without ever exposing what anyone answered.

Counts, never identities

A de-identified view of where your applicants sit in the review process — counts only.

Take the data with you

Export a study’s daily demand metrics for your own analysis and reporting.

A calm weekly recap

A short weekly email summarizing the past week’s demand for your studies — skipped on quiet weeks, never noise.

Referral to randomization

See each study’s applicants move from applied to contacted to in-screening to randomized — one clear funnel per study, current as outcomes are recorded.

Where screening loses people

The share of screened applicants found ineligible, per study — so you can see how cleanly your referrals convert at the screening visit. The rate stays hidden until there are enough decisions to mean something.

How fast referrals convert

Median and average days from an application to a randomized participant — the speed signal behind your enrollment timeline.

See the funnel at all times

Every referral as an opaque, de-identified reference — its current stage, how long it’s been in the funnel, and when it last moved. The full picture, always current, never an identity.

Past enrollment, into milestones

Once patients enrol, see how many complete the study versus discontinue — a retention rate that fills in as outcomes are recorded.

Your whole program in one view

Every study you’ve claimed rolled into one funnel, with a blended screen-fail rate, median time to randomization, retention, and a live referral tracker across studies.

Where your sites are

Every site on your study mapped to states and countries, with the spread at a glance — straight from the registry.

Demand vs. your footprint

Where patients searching your condition area are concentrated, overlaid on your sites — so the states with demand and no nearby site stand out as activation candidates.

Can this protocol enrol?

Demand, where the pre-screen loses people, geographic spread, and how referrals convert — synthesised into one plain read to ground a feasibility conversation.

Reach underrepresented communities

We help design outreach that reaches underrepresented and underserved populations — through geographic targeting, plain-language materials, and advocacy relationships. An approach, grounded in real demand, not a demographic dataset we don’t hold.

The whole disease area

Patient attention rolled up across the specialties and conditions you work in — not just one study — with rolling windows and trends.

All studies, one market view

Every study across every therapeutic area you follow, ranked by where demand is moving.

Where the patients are

Where interested patients are concentrated, to inform site selection and activation — scoped to your program.

Pressure-test a protocol

Where criteria lose otherwise-interested patients, so you can refine eligibility before it locks.

Who else wants your patients

The recruiting trials closest to yours by design and patient area, surfaced from the whole registry — phase, sponsor, design overlap, and where their sites are.

How you stack up against peers

Where your study sits among the recruiting trials most like it — enrollment target, number of sites, and how long it’s been recruiting, all registry facts — with patient interest on Clin2 as a secondary signal. A read for a conversation, not a performance score.

How crowded your pool is

A contention read across the competing set — how many, how similar, and how much site geography they share with you — so competitive risk is quantified.

Demand vs. competition by state

Each of your site states scored on patient demand against competing trials there — a positioning signal to focus activation. A current-data outlook, not a performance prediction.

Plain analysis, with suggestions

A written read of the landscape with concrete risks and suggestions — a starting point for your team, grounded in the data, never a recommendation we can’t stand behind.

Where to build relationships

A starting map of the advocacy organizations, patient communities, and channels in your disease area, with ways to engage — the relationship layer that compounds over time.

Know when interest jumps

We watch view traffic for your studies and flag an unusual rise over a typical week.

Whole-area surge watch

The same watch across the specialties and conditions you follow — hear when an area is heating up, not just one study.

However you want to hear it

A digest email when something moves, plus an in-portal feed with the numbers behind each alert.

Only genuine pickups

Thresholds and a cooldown mean alerts fire only on real, meaningful movement — you’re never spammed.

Opted-in, already oriented

Introductions to patients who match a study’s criteria and have explicitly opted in to be contacted.

Packets to the right contact

A patient’s completed pre-screen packet delivered to the right site contact, gated behind their explicit consent.

Design against real demand

Test eligibility and geography against how patients actually search, before a protocol is locked.

Place studies where demand is

Use demand by area to place studies and activate sites where interested patients already are.

Materials patients understand

Patient-facing summaries and pre-screen questions written in the same clear voice as the rest of Clin2.

Nothing shared without consent

Nothing identifiable about a patient reaches a sponsor or site without that person’s explicit, recorded, study-specific consent.

Aggregate counts only

Everything in your portal is aggregate counts. Identifiable health answers are segregated and access-controlled, never mixed into analytics.

Accountability by design

Every privileged access to identifiable health data is logged.

Patients stay in control

Patients can export and hard-delete their data, including everything they told us — respected throughout the system.

Compliant from day one

Architected for consumer-health-data laws (e.g. Washington’s My Health My Data Act) and the HIPAA relationships that site and sponsor work can trigger.