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Completed

NCT Number: NCT02593604

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

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).

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Key information

Conditions

Hidradenitis Suppurativa Bacterial Infections Bacterial Infections and Mycoses Hidradenitis Infections Skin Diseases Skin Diseases, Bacterial Skin Diseases, Infectious Skin and Connective Tissue Diseases Suppuration Sweat Gland Diseases Wide Excision

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Schleswig-Holstein

Lübeck, Schleswig-Holstein, 23538, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Non-compliance

Treatment and study plan

Primary outcomes

  1. Quality of Life (WHOQOL-BREF)

    Time frame: 2 years postop

    Quality of Life is checked by WHOQOL-BREF

  2. Quality of Life (DLQI)

    Time frame: 2 years postop

    Quality of Life is checked by DLQI

  3. Quality of Life (FLQA-d)

    Time frame: 2 years postop

    Quality of Life is checked by FLQA-d

  4. Quality of Life (Skindex)

    Time frame: 2 years postop

    Quality of Life is checked by Skindex

Secondary outcomes

  1. Sexual Function

    Time frame: 2 years postop

    Sexual Function is checked by IIEF (male) and FSFI (female)

  2. Demographic Parameters

    Time frame: 2 years postop

    Patients' history

  3. Smoking

    Time frame: 2 years postop

    Smoking

  4. Weight and height

    Time frame: 2 years postop

    Weight and height

  5. Wound assessment

    Time frame: 2 years postop

    Localization, Hurley Stage, pain before operation

Sponsors and collaborators

Lead sponsor

University Hospital Schleswig-Holstein

Other

Collaborators

  • Fachklinik Hornheide an der Universität Münster

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Nov 2, 2015
Registry last updated
Oct 12, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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