Quality of Life After Wide Surgical Excision in Patients With Hidradenitis Suppurativa

NCT ID: NCT02593604

Last Updated: 2017-10-12

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

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-03-15

Study Completion Date

2017-04-15

Brief Summary

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Patients undergoing wide surgical excision of their hidradenitis suppurativa areas are asked by telephone about their quality of life by standard questionnaires (WHOQOL-BREF, DLQI, Skindex, MHF, FLQA-d) and their sexual function (FSFI, IIEF).

Detailed Description

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Conditions

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Hidradenitis Suppurativa Wide Excision

Keywords

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Hidradenitis suppurativa Wide excision Quality of Life Sexual Function

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Hidradenitis suppurativa that was wide excised in 2013 in Fachklinik Hornheide
* Agreed to retrospective analysis and questionnaires

Exclusion Criteria

* Non-compliance
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fachklinik Hornheide an der Universität Münster

OTHER

Sponsor Role collaborator

University Hospital Schleswig-Holstein

OTHER

Sponsor Role lead

Responsible Party

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Tobias Kisch

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tobias Kisch, MD

Role: STUDY_DIRECTOR

University of Schleswig-Holstein, Campus Lübeck, Germany

Locations

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University of Schleswig-Holstein

Lübeck, Schleswig-Holstein, Germany

Site Status

Countries

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Germany

Other Identifiers

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U1111-1176-0162

Identifier Type: OTHER

Identifier Source: secondary_id

14-015

Identifier Type: -

Identifier Source: org_study_id