Validation of Swedish Short PROM för Venous Insufficiency

Karolinska Institute

Status: Completed

Conditions: Quality of Life; Change After Treatment; Superficial Venous Insufficiency

Treatments: Other: patient reported outcome measure

Study type: Observational

Funder types: Other

Identifiers

NCT04304937

2017/1824 - 31/2

Details and patient eligibility

About

Validation of a new short Swedish patient reported outcome measure for superficial venous insufficiency. Analysis of its capacity to measure quality of life and its responsiveness to change caused by treatment.

Enrollment: 257 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• agrees to participate, diagnosed with superficial venous insufficiency C2-C6

Exclusion criteria

• does not want to participate, less than C2, does not submit the answered questionnaires

Trial design

257 participants in 2 patient groups

Cohort 1

Description:

test-retest at baseline and 7 days later

Treatment:

Other: patient reported outcome measure

Cohort 2

Description:

test at baseline and 8 weeks post treatment

Treatment:

Other: patient reported outcome measure