Clinical Trials Directory

Trials / Unknown

UnknownNCT04660786

Intralesional Vitamin D in Alopecia Areata

Intralesional Vitamin D3 Injection in Treatment of Alopecia Areata: A Novel Approach

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Alexandria University · Academic / Other
Sex
All
Age
10 Years
Healthy volunteers
Accepted

Summary

To evaluate the efficacy and safety of intralesional injection of vitamin D3 versus intralesional injection of corticosteroids in treatment of alopecia areata. this will be carried out on 40 patients who attend hair outpatient clinic, department of dermatology, Faculty of medicine, Alexandria University, Egypt. The patients will be randomly assigned into two groups (A and B), each group contains 20 patients. Patients will be blindly subjected to intralesional injection of triamcinolone acetonide (5mg/ml) using sterile saline for dilution every 4 weeks for 3 sessions (11,12) or intralesional injection of vitamin D (an aqueous preparation of cholecalciferol (Devarol® ampoule 200,000 IU/2 mL, Memphis, Egypt) (2.5 mg/mL) every 4 weeks for 3 sessions. The maximum total amount of vitamin D3 injected into a patient in 1 session will be 5 mg Injection will be preceded by topical anaesthesia under occlusion for 30 minutes.

Conditions

Interventions

TypeNameDescription
DRUGtriamcinolone acetonidelocal immunosuprresent
DRUGvitamin Dlocal immunomodulator

Timeline

Start date
2021-11-01
Primary completion
2022-12-01
Completion
2022-12-01
First posted
2020-12-09
Last updated
2021-07-26

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04660786. Inclusion in this directory is not an endorsement.