Livedoid Vasculopathy: Strong Association With Smoking, Weak Association With Thrombophilia

NCT ID: NCT05878327

Last Updated: 2023-05-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

15 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-08-31

Study Completion Date

2015-06-30

Brief Summary

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A screening of patient histories at the clinics of Dermatology of the universities of Zurich, Basel and Bern is performed in order to identify patients with a history of Livedoid vasculopathy. Patients with a history of livedoid vasculopathy are asked to participate in the study. After reading the patient information and if the informed consent is signed patients are included in the study. Patients are questioned about their smoking history and blood is drawn in order to perform a screening for thrombophilia.

Detailed Description

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A screening of patient histories at the clinics of Dermatology of the universities of Zurich, Basel and Bern is performed in order to identify patients with a history of Livedoid vasculopathy. Patients with a history of livedoid vasculopathy are asked to participate in the study. The presence of Livedoid vasculopathy must be confirmed by a histologic specimen. After reading the patient information and if the informed consent is signed patients are included in the study. Patients are questioned about their smoking history and blood is drawn in order to perform a screening for thrombophilia. The presence of a history of smoking and thrombophilia is compared to the general Swiss population.

Conditions

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Livedoid Vasculitis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Thrombophilia screening

Patients with livedoid vasculopathy. Investigated by thrombophilia screening

Thrombophilia screening

Intervention Type OTHER

No intervention. Blood is drawn for analysis.

Interventions

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Thrombophilia screening

No intervention. Blood is drawn for analysis.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* History of livedoid vasculopathy

Exclusion Criteria

* Diagnosis was not proved by biopsy specimen
* A different reason than livedoid vasculopathy has been found for the symptoms of the patient
* No informed consent by the patient
Minimum Eligible Age

10 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Juerg Hafner, Prof, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Zurich, Dept. of Dermatology

Locations

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University hospital of Basel

Basel, , Switzerland

Site Status

University hospital of Bern

Bern, , Switzerland

Site Status

University hospital Zurich

Zurich, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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KEK-ZH-Nr. 2013-0301

Identifier Type: -

Identifier Source: org_study_id

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