Actively Recruiting
Quantification of Calcinosis Cutis Disease Burden Using Computed Tomography Images
Led by Yale University · Updated on 2026-02-17
56
Participants Needed
1
Research Sites
37 weeks
Total Duration
On this page
Sponsors
Y
Yale University
Lead Sponsor
N
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main purpose of this study is to develop sensitive radiographic measurement techniques that can be used as outcome measures along with patient-reported outcome instruments in clinical trials of calcinosis cutis treatments, and potentially be used to assess disease course and treatment response in clinical practice. The goal is to test the performance of the software.
CONDITIONS
Official Title
Quantification of Calcinosis Cutis Disease Burden Using Computed Tomography Images
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Scleroderma/systemic sclerosis patient with diagnosed calcinosis cutis who will be clinically treated with STS as part of standard care
- 18 years of age or older
- Meets 2013 American College of Rheumatology criteria for systemic sclerosis diagnosis (diffuse or limited)
- Receiving clinical care at Yale clinics
You will not qualify if you...
- Unable to provide informed consent
- Currently pregnant or nursing
- Patients with a calcinosis region of interest larger than 6 cm
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Yale Scleroderma Program
New Haven, Connecticut, United States, 06520
Actively Recruiting
Research Team
C
Crystal Cheung
CONTACT
D
Diane Documet
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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