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Clinical Trial Summary

This study is performed to consider the safety and healing ability of diosmin in patients with systemic sclerosis (scleroderma) and open sores on their fingers (digital ulcers). Two (2) out of three (3) participants will receive active product. The participants will have four (4) visits over eight (8) weeks. Physical exams and photos will be performed. A variety of questions will be asked describing level of pain and lifestyle changes.


Clinical Trial Description

This study is performed to consider the safety and healing ability of diosmin in patients with systemic sclerosis (scleroderma) and open sores on their fingers (digital ulcers). The study will include 21-45 participants randomly given active product or inactive product (placebo). Two (2) out of every three (3) participants enrolled will receive active product. The participants will have four (4) visits over eight (8) weeks. At each visit physical exams and photos will be performed. Each person will also be asked a variety of questions describing level of pain and any changes to their lifestyle. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06256575
Study type Interventional
Source Primus Pharmaceuticals
Contact Lukban
Phone (480) 483-1410
Email jlukban@primusrx.com
Status Not yet recruiting
Phase N/A
Start date July 15, 2024
Completion date July 15, 2025

See also
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