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Clinical Trials/RBR-9jwgkv
RBR-9jwgkv
Recruiting
未知

Efficacy and safety of Percutaneous Collagen Induction by Needles in the treatment of Frontal Fibrosing Alopecia

Hospital Universitário Walter Cantídeo Universidade Federal do Ceará0 sitesSeptember 28, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Hospital Universitário Walter Cantídeo Universidade Federal do Ceará
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 28, 2020
End Date
TBD
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
Hospital Universitário Walter Cantídeo Universidade Federal do Ceará

Eligibility Criteria

Inclusion Criteria

  • Patients with clinical diagnosis of Frontal fibrosing alopecia will be selected, including those with increased frontotemporal recess, associated or not with follicular papules and rarefaction of eyebrows; or histopathological diagnosis compatible with frontal fibrosing alopecia with follow up appointments at the Dermatology Department of Walter Cantideo University Hospital. Patients must be aged between 18 and 70 years old and must sign who the Informed Consent Form (ICF), with availability to attend periodic appointment evaluations.

Exclusion Criteria

  • Patients with the following conditions will be excluded: Pregnancy; Vitiligo, psoriasis or other skin diseases that present Koebner's phenomenon (development of chronic dermatosis in trauma areas); Active infections in the areas to be treated with microneedling; Presence of keloids in previous scars; History of allergy to topical or injectable anesthetic; Patients with psychiatric disorders or other clinical diseases that contraindicate the procedure; Patients who refuse to sign the Informed Consent Form (ICF) or who are unable to attend to periodic appointment evaluations.

Outcomes

Primary Outcomes

Not specified

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