Topical Vitamin D in Acute Graft Versus Host Disease of the Skin



Status:Recruiting
Conditions:Orthopedic, Hematology
Therapuetic Areas:Hematology, Orthopedics / Podiatry
Healthy:No
Age Range:Any - 35
Updated:2/13/2019
Start Date:March 15, 2017
End Date:December 2020
Contact:Elizabeth Nelson
Email:elizabeth.nelson@cchmc.org
Phone:513-636-1313

Use our guide to learn which trials are right for you!

Clinical Effectiveness of Calcipotriene in Acute Graft Versus Host Disease of the Skin: A Pilot Study

The purpose of this study is to evaluate the efficacy of Calcipotriene cream. This is a
synthetic vitamin D3 derivative for topical use. It is used to treat grade 1-3 acute skin
graft versus host disease (GVHD) in hematopoietic stem cell transplant (HSCT) recipients.
Calcipotriene will be used as the exclusive topical therapy in addition to standard of care
GVHD treatment prescribed for the study subject by the primary physician.

Acute skin GVHD affects about one third of pediatric and adult transplant recipients. Chronic
GVHD (cGVHD) affects 40-60% of adult patients who have undergone allogeneic HSCT. It is a
major cause of non-relapse mortality and morbidity. Systemic prednisone is the first-line
treatment for cGVHD; however, about one-half of all patients do not respond to this initial
therapy, and there is no standard second-line therapy. Immunosuppressive therapy used for
treatment of GVHD brings significant risk of infection, poorly affecting clinical outcomes.

Vitamin D affects immunoregulation, fibroblast proliferation, collagen synthesis and
endothelial cell function, and the investigators hypothesize that topical vitamin D
application will have a positive effect on acute and chronic skin GVHD. The investigators
hypothesize that topical vitamin D cream may restore normal cell function and decrease the
use of steroid creams in acute GVHD of the skin.

Inclusion Criteria:

- HSCT recipients with acute Grade I through III GVHD based on Glucksberg criteria.
Recipients of multiple transplants are still eligible to participate in this research
study.

- Each study subject is to have calcium and vitamin D level prior to starting study, if
not obtained within 30 days of beginning treatment.

Exclusion Criteria:

- Patient with active cellulitis at the start of the treatment.

- Patients with hypercalcemia or vitamin D levels above 100 μg/L.

- Patients with known allergy to any of the topical therapy components.

- Patients who have received previous treatment with topical vitamin D cream.
We found this trial at
1
site
3333 Burnet Avenue # Mlc3008
Cincinnati, Ohio 45229
 1-513-636-4200 
Principal Investigator: Gregory Wallace, DO
Phone: 513-636-1313
Cincinnati Children's Hospital Medical Center Patients and families from across the region and around the...
?
mi
from
Cincinnati, OH
Click here to add this to my saved trials