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Clinical Trials/NCT02147262
NCT02147262
Unknown
Not Applicable

Inflammatory Proteins,Gene Polymorphisms, and Transcriptome Profiles in Patients With Chronic Atrophic Acrodermatitis

University Medical Centre Ljubljana1 site in 1 country50 target enrollmentJuly 2013

Overview

Phase
Not Applicable
Intervention
doxycycline orally, 100 mg, bid, 14 days
Conditions
Chronic Atrophic Acrodermatitis
Sponsor
University Medical Centre Ljubljana
Enrollment
50
Locations
1
Primary Endpoint
inflammatory proteins in patients with chronic atrophic dermatitis
Last Updated
8 years ago

Overview

Brief Summary

The main objective of this study is to characterize the inflammatory proteins, gene polymorphisms, and transcriptome profiles in patients with chronic atrophic dermatitis to gain better insight into pathogenesis of chronic infection with Borrelia burgdorferi sensu lato.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
July 2020
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Franc Strle

M.D., PhD

University Medical Centre Ljubljana

Eligibility Criteria

Inclusion Criteria

  • chronic atrophic dermatitis in patients \>18 years

Exclusion Criteria

  • Not provided

Arms & Interventions

ACA-doxy 14 days

patients with chronic atrophic acrodermatitis treated with doxycycline for 14 days

Intervention: doxycycline orally, 100 mg, bid, 14 days

ACA-doxy 28 days

patients with chronic atrophic acrodermatitis treated with doxycycline for 28 days

Intervention: doxycycline orally, 100 mg, bid, 28 days

Outcomes

Primary Outcomes

inflammatory proteins in patients with chronic atrophic dermatitis

Time Frame: up to 24 months

The inflammatory immune profiles will be assessed using Luminex to measure the expression of cytokines and chemokines representative of innate and adaptive TH1, TH2, TH17, and B cell responses.

Secondary Outcomes

  • clinical characteristics of patients with chronic atrophic dermatitis treated with doxycycline for 14 or 28 days(at enrollment, at 2, 6 12 and 24 months follow-up)

Study Sites (1)

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