Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 8:03 PM
Ignite Modification Date:
2025-12-24 @ 8:03 PM
NCT ID:
NCT01918904
Eligibility Criteria:
Inclusion Criteria:
* Patients seen by the Division of Rheumatology at Loyola Outpatient Center in Maywood, Illinois (IL), Oak Brook Terrace Outpatient Center in Oakbrook, IL, and Burr Ridge Outpatient Center in Burr Ridge, IL.
* Male and female patients 18 years old and above
* Patients with at least 2 distinct calcinosis cutis lesions separated by at least 10 inches, that are a minimum of 2 millimeters (mm) in diameter, and identifiable on physical exam and ultrasound, such that one lesion may be used as an internal control lesion
* Patients on calcium channel blockers, bisphosphonates, prednisone, and colchicine will be included
Exclusion Criteria:
* Patients with calcinosis cutis lesions that appear actively infected (i.e., exhibiting purulent drainage and malodor) will not be included
* Patient with concomitant use of systemic intravenous sodium thiosulfate for treatment of calciphylaxis will not be included
* Patients with hypercalcemia will not be included
* Patients who are pregnant or breastfeeding will not be included
* Patients who are allergic to sulfa and/or zinc will not be included
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01918904
Study Brief:
Protocol Section:
NCT01918904