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Lichen Sclerosus - the Influence on Quality of Life

V

Vendsyssel Hospital

Status

Completed

Conditions

Lichen Sclerosus

Treatments

Other: Standard care and sexological counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT03419377
RHN_DMK_02

Details and patient eligibility

About

A randomised controlled trial of Lichen Sclerosus in a period of six months measuring Quality of Life and sexuality among women with Lichen Sclerosus.

Full description

The patients are randomized to an intervention Group and a control Group. The intervention gets 6-8 visits with clinical sexologist and the control Group is having the usual care.

Enrollment

158 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with Lichen Sclerosus
  • Age over 18 years

Exclusion criteria

  • Patients who does not understand or speak Danish
  • Patients with a psychiatric diagnosis and can not follow the course

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

158 participants in 2 patient groups

Standard care and sexological counseling
Experimental group
Description:
Standard care including gynecological examination and 6-8 sexological consultations.
Treatment:
Other: Standard care and sexological counseling
Standard care
No Intervention group
Description:
Standard care including gynecological examination.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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