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Alopecia Areata | The Comparison Study of Intralesional Botulinum Toxin A and Corticosteroid Injection for Alopecia Areata

Alopecia Areata research study

What is the primary objective of this study?

Alopecia areata is one of the most common cause of non-scarring alopecia. The pathogenesis is still unclear, however, it is believed to be an autoimmune disease. This disease is not a life-threatening condition but it has a significant psychological impact to patient's quality of life. Many triggers have been proposed such as viral infection, stress and neurologic factors. There are many studies show the correlation between disease activities and neurotransmitters level. Substance P and calcitonin gene-related peptide play major role in early stage of disease. These substances cause imbalance of CD4/CD8 lymphocyte in pathologic site and loss of immune privilege of hair follicles. The conventional treatment of alopecia areata with intralesional corticosteroid injection might treat the end of pathogenesis process. There is no therapeutic intervention for the origin of disease. Fortunately, botulinum toxin A could be a novel treatment of alopecia areata. The botulinum toxin A demonstrates inhibition release of substance P in many publications. To sum up, the treatment of alopecia areata with intralesional corticosteroid injection still be a standard treatment, nevertheless, patients have to receive this treatment every month until regrowth of scalp hair. Corticosteroid injection have several side effects, for example, skin atrophy, pigmentary change and hypothalamic-pituitary-adrenal axis suppression. Moreover, injection pain is also affect to psychological aspect . This study purpose is to evaluate the efficacy of botulinum toxin A for alopecia areata and reduce corticosteroid side effects, as well as, others opportunity cost. There is no prospective, randomized-controlled trial of comparison study between botulinum toxin A injection and corticosteroid injection for alopecia areata, therefore, investigators conduct this study for the greatest benefit to alopecia areata patients and for the future research in disease etiology.

Who is eligible to participate?

Inclusion criteria - Patients must be above 18 years old - Newly diagnosed with multiple alopecia areata - Patient has lesions on the both side of the scalp. - Lesions's diameter varies between 2-6 cms Exclusion criteria - Having active scalp inflammation - Allergic to botulinum toxin A or human albumin - Receiving any medication that interfere efficacy of botulinum toxin such as macrolides antimicrobial agents or neuromuscular medications - Diagnosed with neuromuscular diseases such as Myasthenia gravis - Pregnant, breast feeding, plan to pregnant patients

Which medical condition, disease, disorder, syndrome, illness, or injury is researched?

Alopecia Areata

Study Interventions

Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.

Drug:Botulinum toxin type AUsing concentration at 2 units per 0.1 of dilution with normal saline Injection in the first visit and follow up at 1 week, 1,2,3 and 4 months after injection

Drug:Triamcinolone acetonideUsing concentration at 10 mg/ml and equal amount of botulinum toxin A dilution

Study Arms

Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.

Botulinum toxin AAt first visit, patients will be randomized by blocked randomization into 2 sides of scalp. Experimental side will be injected with botulinum toxin A ( Botox) 2 units per 6.05 cm2 of lesion ( Concentration 2 units of Botox per 0.1 ml of normal saline ).

Triamcinolone acetonideAt visit0, patients will be injection with triamcinolone acetonide concentration at 10 mg/ml on the comparison side

Study Status

Unknown status

Start Date: November 2009

Completed Date: February 2013

Phase: N/A

Type: Interventional

Design:

Primary Outcome: The percentage of terminal hair regrowth after intralesional botulinum toxin A injection

Secondary Outcome: Possible side effects of intralesional botulinum toxin a injection

Study sponsors, principal investigator, and references

Principal Investigator: Rattapon Thoungtong, MD.

Lead Sponsor: Siriraj Hospital

Collaborator:

More information:https://clinicaltrials.gov/show/NCT00999869

Safavi KH, Muller SA, Suman VJ, Moshell AN, Melton LJ 3rd. Incidence of alopecia areata in Olmsted County, Minnesota, 1975 through 1989. Mayo Clin Proc. 1995 Jul;70(7):628-33.

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