Foundation for Sarcoidosis Research Advanced Cures Registry (FSR-SARC Registry)
Foundation for Sarcoidosis Research · NCT06234384
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 7+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 6833
- US sites recruiting
- 1
- Study start
- July 2013
- Record last updated
- September 19, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of the study is to create a longitudinal record of patient reported outcomes for people living with sarcoidosis that maintains privacy. Patients report on the following: demographics, disease symptoms, diagnostic journey, provider experience, disease treatment, and burden of disease. Patients can also link their Electronic Health Records (EHR). The goal is to create a natural history of sarcoidosis, support research, and better understand the needs of the sarcoidosis community.
Being studied: Sarcoidosis diagnosis
Conditions: Sarcoidosis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- English speaking
- Consent
- Sarcoidosi diagnosis -
Exclusion Criteria
NONE
Recruiting US locations
Foundation For Sarcoidosis Research
Chicago, IL 60654
Site contact: Tricha Shivas, MBe · 312-241-0400 · tricha@stopsarcoidosis.org
Study contacts (from the official record)
- Leslie Serhuck, MD MA Mbioethics · 312-341-0500 · info@stopsarcoidosis.org
- Tricha Shivas, MBe · 312-341-0500 · tricha@stopsarcoidosis.org
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