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Mayo Clinic Rare and Undiagnosed Disease Hackathon

This study aims to create a special collection of biological samples (biospecimens) and health information (data repository) at Mayo Clinic. This collection will help doctors better understand and diagnose rare and undiagnosed conditions. You might be able to join if you have a rare or undiagnosed condition, have received care at Mayo Clinic, and have had genetic testing that didn't provide a diagnosis. The study is looking to enroll 50 participants. The main goal is to see if it's possible to successfully set up this biospecimen and data collection within one year. The current recruitment status is unclear.

Study design
This is an observational study, meaning researchers will collect information without giving any specific treatments. It plans to enroll 50 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The study aims to establish the biospecimen and data repository, with feasibility measured at 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07714161

The Mayo Clinic Rare and Undiagnosed Disease Hackathon

Not Yet Recruiting
Not specifiedAll AgesObservational
Mayo Clinic
~50 participants
Updated 2026-07-20 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility of establishing a biospecimen and data repository
Measured over 1 year

Conditions

Undiagnosed Diseases
Genetic Diseases
Rare Diseases

Explore related trials

Genetic DisorderRare DisorderUndiagnosed Diseases

Where it's being run

1 sites across 1 states
Minnesota1

Study leadership

  • Eric Klee, Ph.D. · PRINCIPAL_INVESTIGATOR · Mayo Clinic

Who to contact

Mayo Hackathon Team
[email protected]
507-738-7890
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Patients receiving or having received care at Mayo Clinic with rare or undiagnosed conditions; of any age (including pediatric); who can provide informed consent or have a legally authorized representative (LAR).
Patients who have undergone prior standard genetic testing that was non-diagnostic; and who are nominated by a Mayo Clinic clinician sponsor and selected by the Study Team.

Exclusion

Patients with a confirmed molecular or clinical diagnosis that fully explains their phenotype
Patients unable to provide consent and without a legally authorized representative (LAR)
Patients for whom sample collection cannot be coordinated
Patients enrolled in a clinical trial that precludes ancillary genomic research (evaluated on a case-by-case basis)
Prisoners will not be included in this study

What this trial measures

  • Feasibility of establishing a biospecimen and data repository1 year

    Number of enrolled participants who complete all planned repository workflow steps, including eligibility confirmation, informed consent, biospecimen collection, clinical data abstraction, research data generation, and multidisciplinary Hackathon case review.