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Comparison of two treatment methods for Alopecia Areata (Patchy hair loss)

A Comparative therapeutic evaluation of two treatment modules in Alopecia areata. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110136
Enrollment
40
Registered
2026-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L638- Other alopecia areata

Interventions

Intervention1: Majoon-e-Chobchini, Microneedling: Microneedling and Majoon-e- chobchini will be given for the duration of 10 weeks. Microneedling include needles, characterized by their micron-sized s

Sponsors

Ajmal khan tibbiya college and hospital Department of Amraz e jild wa zohrawiya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1-Clinically diagnosed cases of Alopecia areata. [characterized by patchy, non-scarring hairloss with smooth scalp surface on inspection,presence of exclamation mark hairs on tricoscopy, History of associated Autoimmune -condition(s). 2-Clinically stable patients. 3-Patients of either gender. 4-Patients between 18-60 Years of age. 5-Patient not on any concomitant therapy. 6-Patient who has left the treatment at least 2 months back. 7-Patient willing to sign the written consent proforma. 8-Patient who follows the protocol.

Exclusion criteria

Exclusion criteria: 1-Subjects below 18 years and above 60 years. 2-Subjects with a known history of any autoimmune disorders. 3-K/C/O diabetes, bleeding disorder or patient on anticoagulant and /or antiplatelet therapy. 4-Subjects who had received either Anti-androgenic medications or drugs causing hypertrichosis or hypotrichosis, use of Ritlecitinib or other JAK inhibitors or topical minoxidil within 01 months prior to enrolment. 5-Subjects with surgical correction of scalp hair loss (hair transplant or scalp reduction). 6-Subjects with a known history of Seborrheic dermatitis, Lichen planopilaris, Scalp psoriasis, Tinea Capitis, Male androgenic alopecia, Alopecia Totalis,A.universalis, scarring alopecia Trichotillomania . 7-Subjects who fail to comply the study protocol or stop treatment midway during protocol will not be included in final data analysis but they will be reported separately.

Design outcomes

Primary

MeasureTime frame
A)Severity of Alopecia Tool (SALT) score B)Trichoscopy C)Alopecia Areata symptom impact scale (AASIS) D)Photographs of lesionTimepoint: At 15th, 30th, 45th, 60th, 75th day.

Secondary

MeasureTime frame
Dermatology Life Quality of LifeTimepoint: At 15th, 30th, 45th, 60th, 75th day.

Countries

India

Contacts

Public ContactDr Shabnam Jahan

Ajmal khan tibbiya college

aqdas2005@gmail.com9412329198

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026