FOR HEALTHCARE PROFESSIONALS

Help a Patient Explore a Clinical Research Opportunity

ProConXol can route an inquiry to an appropriate site or study team. A referral does not confirm eligibility, and the patient remains free to decline or withdraw from consideration at any time.

Start a Referral Inquiry

WHAT HAPPENS NEXT

A careful, study-specific process.

01

Initial review

A trained team member reviews the non-sensitive information and determines whether there may be a relevant, actively recruiting study or site.

02

Patient permission

Before discussing identifiable health information or contacting the patient, the appropriate permission and privacy process must be followed.

03

Study-specific screening

If there may be a match, the authorized study team explains the next screening steps and determines eligibility under the protocol.

04

Informed decision

The patient receives information about purpose, procedures, risks, potential benefits, alternatives, time, privacy, and voluntary participation.

FOR PATIENTS & FAMILIES

Ask about research opportunities without sending sensitive information.

You may contact ProConXol directly, but please do not send medical details through a general website form. Research is not a substitute for emergency or routine medical care. For medical questions, contact a healthcare professional; for an emergency, contact local emergency services.

Ask About Opportunities

REFERRAL QUESTIONS

Important distinctions for patients and clinicians.

Does a referral guarantee participation?+

No. Eligibility is determined by the study’s approved inclusion and exclusion criteria and the authorized study team.

Will the referring clinician remain involved?+

The patient’s usual care remains with the patient and healthcare team. Study communication depends on authorization, the protocol, and applicable privacy requirements.

Does participation guarantee a medical benefit?+

No. Research may or may not provide direct benefit. The study team explains potential risks, benefits, alternatives, and requirements during informed consent.