- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05954104
Evaluation of the Effect of Topical Calcipotriol Versus Platelet-Rich Plasma
Evaluation of the Effect of Topical Calcipotriol Versus Platelet-Rich Plasma Versus Combined of Both on Serum Adiponectin Level in Alopecia Areata
Alopecia areata (AA) is a common, immune-mediated non scarring alopecia and can be associated with severe psychological consequences . Alopecia Areata affects 2% of the global population. Alopecia Areata prevalence is lower in adults than children, is increasing over time, and significantly differs by region.
Its etiology is unknown but it was hypothesized to be an autoimmune disease mediated by T-lymphocytes. It has been suggested that inflammatory T cells induce growth arrest in hair bulbs in the anagen phase of the hair cycle . Cytotoxic T cells secrete tumor necrosis factor, granzymes, and Fas ligand which trigger apoptosis in affected hair follicle and disrupt hair growth
Study Overview
Detailed Description
Clinically, Alopecia Areata presents as a well-circumscribed patch of sudden hair loss. It affects any hair bearing area. The most common affected site is the scalp .
Dermoscopy is a highly valuable tool in diagnosis and follow-up of Alopecia Areata. The most common trichoscopic features of Alopecia Areata are yellow dots, micro exclamation mark hairs, tapered hairs, black dots, broken hairs, and regrowing upright or regrowing coiled hairs .
The diagnosis of alopecia areata is commonly established based on clinical appearance, In cases of ambiguity, trichoscopy may be useful to avoid invasive procedures such as biopsy.
Treatment of alopecia areata is dependent on age of patient as well as the extent and duration of scalp involvement. Treatments include steroids, topical immunotherapy, topical minoxidil, anthralin, and immunosuppressants. Each case must be dealt with on a customized individual basis.
Platelets rich plasma (PRP) is an autologous preparation of platelets in concentrated plasma. Injection of PRP improves cutaneous ischemic conditions, increases vascular structures around hair follicles and induces the proliferation of dermal papilla cells by up regulating fibroblast growth factor 7 (FGF-7) .Anagen-associated angiogenesis has been suggested as one of the important factors in active hair growth, due to the secretion of vascular endothelial growth factor by the keratinocytes of the outer root sheath and fibroblasts of the dermal papilla .
Topical calcipotriol is a vitamin D analogue that regulates keratinocytes proliferation and differentiation. It can induce hair regrowth in Alopecia Areata lesions by regulation of the differentiation of B cells, T cells, dendritic cells, and Toll-like receptor expression. There are few reports evaluating the effect of calcipotriol in Alopecia Areata .
Patients with Alopecia Areata are characterized by an abnormal serum level of adipokines, particularly adiponectin and resistin. Adiponectin may be considered as a marker of severity of hair loss in alopecia areata. Impaired secretion of specific adipokines may play an important and complex role in the pathogenesis of Alopecia Areata and its continuity
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Aswan, Egypt
- Faculty of Dentistary - Aswan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients with non-severe alopecia areata , a severity of alopecia tool (SALT) score up to 2 with less than 50% of scalp involvement.
- No restriction of age , race, nor occupation
Exclusion Criteria:
- Pregnant and lactating women, immunocompromised patients.
- Patients having active scalp inflammation.
- Patients who received systemic treatment for Alopecia Areata in the last 3 months or applied any topical or intradermal treatments in the last 4 weeks .
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A
About 20 patients suffering from Alopecia areata , they will receive topical vit D3 analogue (calcipotriol) 0.005% twice daily for 3 months with follow up
|
To evaluate the efficacy of Calcipotriol on Alopecia Areata.
Other Names:
|
|
Active Comparator: Group B
About 20 patients suffering from Alopecia areata , they will be injected by PRP intra lesional for 3 consecutive sessions 4weeks apart.
|
To evaluate the efficacy of Calcipotriol on Alopecia Areata.
Other Names:
|
|
Active Comparator: Group C
About 20 patients suffering from Alopecia areata they will receive combined therapy ( PRP and topical vit D3 analogue).
|
To evaluate the efficacy of Calcipotriol on Alopecia Areata.
Other Names:
|
|
Active Comparator: Group D
About 20 of Healthy control group .
|
To evaluate the efficacy of Calcipotriol on Alopecia Areata.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Efficacy of topical calcipotriol and platelet Rich Plasma in Alopecia Areata treatment
Time Frame: from baseline to 3 months
|
Evaluating the patients suffering from Alopecia Areata clinically, with Severity of Alopecia Tool (SALT) score.
As score of 0 means no hair loss, while a SALT score of 100 is complete hair loss.
and this evaluation will be done by trichoscopy
|
from baseline to 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
serum adiponectin level.
Time Frame: from baseline to 3 months
|
Compare the effect of topical calcipotriol, PRP, and combination of both on serum adiponectin level.by
doing the ELISA test for Alopecia Areata patients before treatment and 3 months after treatment
|
from baseline to 3 months
|
|
serum Adiponectin level in Alopecia Areata
Time Frame: from baseline to 3 months
|
Compare serum adiponectin level in Alopecia Areata patients with its serum level in healthy control group.by
doing the ELISA test for Alopecia Areata patients before treatment and for healthy control group.
|
from baseline to 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Moustafa Adam, Professor, Department of dermatology , Venerolgy and Andrology Faculty of Medicine Aswan university
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Faten Othman
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.