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Clinical Trial Summary

A study to compare pain differences between using MedJet needle-free drug-delivery system with standard of care treatment for cutaneous T-cell lymphomas and cutaneous B-cell lymphomas in participants.


Clinical Trial Description

Participants will undergo treatments on two morphologically and anatomically matched target lesions, preferably on opposing sides of the body. The first plaque will be treated using standard of care topical bexarotene or nitrogen mustard for participants with CTCL (cutaneous T-cell lymphomas) or intralesional TAC (triamcinolone acetonide) using a syringe/needle with participants with CBCL (cutaneous B-cell lymphomas). The second plaque will be treated using a needle-free injector system. After the treatment, the participants will be followed for another three visits over the course of 4 months to see how the treated areas responded. In order to account for 20% dropout, 11 patients per group (a needle free and a traditional treatment group in CBCL patients and the same two groups in CTCL patients) will be recruited. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05106192
Study type Interventional
Source Case Comprehensive Cancer Center
Contact Amy Johnson, MD
Phone 216-286-7369
Email amy.johnson@uhhospitals.org
Status Not yet recruiting
Phase N/A
Start date June 1, 2024
Completion date February 1, 2025

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