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Efficacy of Jessener Solution Versus Intralesional Steroid in Treatment of Alopecia Areata (AA)

A

Al-Azhar University

Status and phase

Unknown
Early Phase 1

Conditions

Alopecia Areata

Treatments

Drug: Corticosteroids Acting Locally

Study type

Interventional

Funder types

Other

Identifiers

NCT04964349
Ahmed Kadah (Other Identifier)
Alazhar faculty of medicine
Eman Abd-ellatif (Other Identifier)

Details and patient eligibility

About

Alopecia areata is believed to be an autoimmune disease. Treatment primarily relies on intralesional and topical corticosteroids. This study was conducted to evaluate Jessener Solutionas a potential therapeutic modality of Alopecia Areataversusintralesional steroid as regards the efficacy, safety, tolerability, and patients' satisfaction.

Full description

Background Alopecia areata is believed to be an autoimmune disease resulting from a breach in the immune privilege of the hair follicles causing non scarring hair loss.Treatment primarily relies on intralesional and topical corticosteroids.Up till now, there is nouniversally proven therapy that induces and maintains remission of Alopecia Areata in all patients.

Aims The Aim of Study is to evaluate the efficacyof Jessener solution versus intralesional steroid in treatment of Alopecia Areata.

Patients and Methods The study will include 40 patients diagnosed clinically and dermoscopically as Alopecia Areata with more than two patches of alopecia areata were included. Two treatment modalities with intralesional corticosteroid and topical Jessener Solutionas were performed in two randomly selected patches. Three sessions were done, 3 weeks apart and were followed-up for three months. Evaluation was done using Mac Donald Hull and Norris grading system , Serial photographs and dermoscopic , trichoscopic examination every month will be done and patient will be score.

Enrollment

40 estimated patients

Sex

All

Ages

12 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 1.Alopecia Areatamultilocuolaris.2.Age from18-50years old. 3.Wash out period is two months. 4.Ophiasis pattern alopecia areata.

Exclusion criteria

  • Age less than 12 yearsand more than 40years old. 2.Patient under treatment.3.Patients having another dermatological condition affecting thescalpas eczema.4.Patients with psychiatric disorders.5.Pregnant and lactating females.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Intralesional cortisosteroid injection
Experimental group
Description:
Intralesional corticosteroid injection
Treatment:
Drug: Corticosteroids Acting Locally
jessener solution
Experimental group
Description:
topical jessener solution
Treatment:
Drug: Corticosteroids Acting Locally

Trial contacts and locations

1

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Central trial contact

Ahmed pr Elshahid, MD

Data sourced from clinicaltrials.gov

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