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Scientists analyze genetic markers in stored samples to boost personalized medicine

NCT ID NCT07573072

Knowledge-focused Sponsor: Istituto Ortopedico Rizzoli Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at DNA methylation patterns in stored samples from 90 patients with rare skeletal disorders, sarcomas, or inflammatory arthritis. The goal was to better understand these patterns and explore their potential for diagnosis and treatment. The research aimed to improve data sharing and support personalized medicine for these conditions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

90 people

The number who actually took part.

Started

Mar 2025

Finished

Jul 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

patients affected by a rare skeletal disorder, sarcoma, or inflammatory arthritis.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Be a patient with a sample stored in one of the biobanks belonging to the CRB IOR * Have one of the following conditions: a rare skeletal disorder, sarcoma, or inflammatory arthritis. Exclusion Criteria: * Patients who have refused to consent to the use of their samples or the processing of their data for genetic studies * Patients who have refused to consent to the transfer of their samples outside the IOR

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Conditions

The condition(s) this trial relates to.

arthritic joint disease bone sarcoma osteosarcoma sarcoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Inflammatory articular diseases Rare disorders Sarcoma of bone and connective tissue

Contacts and locations

Locations

  • IRCCS Istituto Ortopedico Rizzzoli

    Bologna, BO, 40136, Italy

More trials for these conditions

Other studies related to the condition(s) this trial covers.