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

NCT02593604 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2017-10-12

No results posted yet for this study

Summary

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).

Conditions

Sponsors & Collaborators

  • Fachklinik Hornheide an der Universität Münster

    collaborator OTHER

  • University Hospital Schleswig-Holstein

    lead OTHER

Principal Investigators

  • Tobias Kisch, MD · University of Schleswig-Holstein, Campus Lübeck, Germany

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-15
Primary Completion
2017-04-15
Completion
2017-04-15

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02593604 on ClinicalTrials.gov