UK clinical trials - updated daily from ClinicalTrials.gov
For Sponsors, CROs & Researchers
TrialConnect connects your clinical trials with pre-qualified, consented patients across the UK. Our AI matching platform handles eligibility pre-screening, patient consent, and site-level routing — so your team spends time on enrolled patients, not screening failures.
Who we work with
Pharma Sponsors
Get your trial in front of actively searching, pre-qualified patients across the UK. We index from ClinicalTrials.gov automatically — and can create custom landing pages, condition-specific campaigns, and targeted outreach for your study.
CROs & Site Networks
Stop relying on slow referral chains. TrialConnect sends you patients who have already been matched against your protocol criteria and have opted in to be contacted.
Academic & NHS Researchers
Most NHS studies struggle with recruitment because patients do not know they exist. TrialConnect makes your study discoverable to patients searching for their condition — automatically, and at no cost to the patient.
Platform capabilities
Receive patients who have already been scored against your eligibility criteria. Our multi-dimensional matching engine reduces screen failures and accelerates enrolment.
As your trial criteria update or new patients join, matches are recalculated automatically. No manual searching, no stale lists.
Deep integration with ClinicalTrials.gov, the ISRCTN registry, and the NIHR portfolio means comprehensive coverage of UK-based trials and NHS sites.
Built from the ground up for UK GDPR compliance. Patient consent, data minimisation, right to erasure — all handled by the platform.
Most trials are already indexed. Getting set up for active matching takes 1–2 weeks.
Your trial is automatically indexed from ClinicalTrials.gov and ISRCTN. No manual data entry needed.
Our parser extracts eligibility rules from your protocol. You can refine or add criteria for tighter matching.
Patients are matched and scored in real-time. Contact pre-qualified patients through the platform when they opt in.
Still have questions? Get in touch — we are happy to talk through specifics.
Patients search for their condition on TrialConnect and complete an interactive eligibility questionnaire. Our matching engine scores them against your protocol criteria in real time. Patients who match and consent to contact are made available to your study team — you never see patients who have not opted in.
We index recruiting trials from ClinicalTrials.gov, the ISRCTN registry, and the NIHR portfolio. If your trial is registered on any of these, it is likely already in our system. We can also add trials directly for studies not yet registered.
Yes. TrialConnect is built for UK GDPR from the ground up. Patients consent explicitly before any data is shared. We practise data minimisation — sponsors see only what is necessary for pre-screening. Patients can withdraw consent and request erasure at any time.
If your trial is already registered on ClinicalTrials.gov, it is likely already indexed. We can have custom matching criteria and a sponsor dashboard set up within 1–2 weeks. For urgent recruitment needs, we offer expedited onboarding.
Pricing depends on the number of trials, complexity of matching criteria, and whether you need custom landing pages. We offer reduced rates for academic and publicly funded studies. Get in touch for a quote.
No. TrialConnect is always free for patients. Our revenue comes from sponsors and research organisations who value pre-qualified, consented patient matches.
Tell us about your trial. We will walk you through the platform, show you matched patient volumes for your indication, and discuss how we can accelerate your recruitment.
No obligation. No spam. We respond within 1–2 business days.
Email us directly to discuss partnership, patient recruitment, or custom integrations.
We typically respond within 1–2 business days. For urgent enquiries, include "URGENT" in the subject line.
No form, no spam — just direct email.
