Volume 6, Issue 3 (Volume 6, Number 3 2015)                   jdc 2015, 6(3): 134-139 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ranjkesh M, Babaeinejad S, Aghazade M, Radmehr A, Anoush B, Fadaei Fooladi D. Comparing the efficacy of basal cell layer suspension implementation alone and in combination with topical calcipotriol in patients with stable vitiligo: A randomized controlled clinical trial. jdc 2015; 6 (3) :134-139
URL: http://jdc.tums.ac.ir/article-1-5133-en.html
1- Department of Dermatology, School of Medicine, Tabriz University of Medical, Tabriz, Iran
2- Department of Dermatology, School of Medicine, Tabriz University of Medical, Tabriz, Iran , medicorelax@yahoo.com
Abstract:   (6097 Views)

Background and Aim: Vitiligo is an skin condition that results in the skin depigmentation. The implementation of a basal cell layer suspension is a novel treatment in cases with recalcitrant vitiligo. In this study, the efficacy of topical calcipotriol on the implementation site with basal cell layer suspension versus basal cell layer suspension application alone was compared.

Methods: In this randomized, controlled clinical trial, 20 patients with recalcitrant vitiligo were randomly allocated in two 10-patient groups, undergoing the implementation of basal cell layer suspension alone (controls) or along with daily application of topical calcipotriol (intervention group). Results and possible complications were compared between the two groups 6 months after initiation of the treatment.

Results: Six months after initiation of the study, 2 patients (20%) in the control group had poor responses, and 8 patients (80%) had moderate/good responses. In the intervention group, 1 patient (10%) showed poor response, and 9 patients (90%) showed moderate/good responses (P>0.05). Complications were trivial and self-limiting.

Conclusion: Although topical application of calcipotriol did not signigicantly change the primary outcome of the study, it was associated with better results and no major side effects.

Full-Text [PDF 286 kb]   (2130 Downloads)    
Type of Study: Research | Subject: Special
Received: 2015/12/20 | Accepted: 2015/12/20 | Published: 2015/12/20

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 , Tehran University of Medical Sciences, CC BY-NC 4.0

Designed & Developed by : Yektaweb