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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02593604

Enrollment

Registered

2015-11-02

Start date

2015-03-15

Completion date

2017-04-15

Last updated

2017-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hidradenitis Suppurativa, Wide Excision

Keywords

Hidradenitis suppurativa, Wide excision, Quality of Life, Sexual Function

Brief 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).

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

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

Exclusion criteria

* Non-compliance

Design outcomes

Primary

Measure	Time frame	Description
Quality of Life (WHOQOL-BREF)	2 years postop	Quality of Life is checked by WHOQOL-BREF
Quality of Life (DLQI)	2 years postop	Quality of Life is checked by DLQI
Quality of Life (FLQA-d)	2 years postop	Quality of Life is checked by FLQA-d
Quality of Life (Skindex)	2 years postop	Quality of Life is checked by Skindex

Secondary

Measure	Time frame	Description
Sexual Function	2 years postop	Sexual Function is checked by IIEF (male) and FSFI (female)
Demographic Parameters	2 years postop	Patients' history
Smoking	2 years postop	Smoking
Weight and height	2 years postop	Weight and height
Wound assessment	2 years postop	Localization, Hurley Stage, pain before operation

Countries

Germany

Outcome results