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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03847441
Other study ID # Alopecia Calcipotiol
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date December 31, 2018

Study information

Verified date March 2019
Source Aswan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Alopecia Areata is a common condition. This study investigated the efficacy of calcipotriol versus Narrow Band Ultraviolet B in treatment of Alopecia areata and their effects on serum vitamin D3 levels.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 14 Years to 40 Years
Eligibility Inclusion Criteria:

- Alopecia Areata of scalp

Exclusion Criteria:

Other causes of alopecias including scarring alopecia, androgenic alopecia, telogen effluvium autoimmune diseases, pregnant and lactating females

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Calcipotriol
Calcipotriol ointment (0.005%)
Device:
Narrow Band UVB
NB-UVB (311nm) phototherapy
Diagnostic Test:
vitamin D3 level
vitamin D3 (ng/ml)

Locations

Country Name City State
Egypt Aswan University Hospital Aswan

Sponsors (1)

Lead Sponsor Collaborator
Aswan University Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical improvement of Alopecia Areata After treatment As assessed by Severity of Alopecia tool (SALT) score calculation of SALT score before and after treatment 3 months
Primary Improvement of serum Vitamin D levels in (ng/ml) after treatment measurement of serum vitamin D before and after treatment 3 months
See also
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Completed NCT00408798 - Treatment of Alopecia Areata of the Scalp With Intradermal Injections of Botulinum Toxin N/A