Your session is about to expire
← Back to Search
Observational for Langerhans Cell Histiocytosis
N/A
Recruiting
Led By Ronald S. Go, M.D.
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* All patients diagnosed with histiocytic disorders and age ≥1 year
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline; post-treatment (estimated up to 2 years, potentially 4 times per year)
Awards & highlights
Study Summary
This study is being done to collect medical and personal histories as well as a samples of blood, other body fluid and/or tumor/disease tissue for current and future research studies on histiocytic disorders.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline; post-treatment (estimated up to 2 years, potentially 4 times per year)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline; post-treatment (estimated up to 2 years, potentially 4 times per year)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in PD-L1 and T-cell Bim expression
Identify molecular markers
Trial Design
1Treatment groups
Experimental Treatment
Group I: ObservationalExperimental Treatment1 Intervention
Patients complete questionnaires and undergo blood and tissue sample collection. Patients' medical records are also reviewed.
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,212 Previous Clinical Trials
3,766,538 Total Patients Enrolled
Ronald S. Go, M.D.Principal InvestigatorMayo Clinic in Rochester
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
Share this study with friends
Copy Link
Messenger