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15% TOPICAL RESORCINOL FOR HURLEY I-II HIDRADENITIS SUPPURATIVA.

F

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Status

Unknown

Conditions

HYDRADENITIS

Study type

Observational

Funder types

Other

Identifiers

NCT04099212
FIS-RES-2018-01

Details and patient eligibility

About

Prospective, observational cross-sectional study to evaluate the response of patients with HS I-II to monotherapy treatment of topical resorcin 15%, taking into account its safety, impact on quality of life and subclinical evolution.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years.
  • Diagnosed with HS Hurley I-II degree.
  • Patients that have at least 1 or more swollen up nodules and/or abscess.
  • Availability of affected region control ultrasound prior to resorcine treatment beginning.

Exclusion criteria

  • Age < 18 years.
  • Number of draining fistula above 20.
  • Patients in active treatment with immunomodulators.
  • Patients in active treatment with antibiotics.

Trial design

40 participants in 1 patient group

Cases
Description:
Patients with HS I-II in monotherapy treatment of topical resorcinol 15%

Trial contacts and locations

1

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Central trial contact

Jaime Cordero Ramos; Carlos García Pérez

Data sourced from clinicaltrials.gov

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