Validation of Swedish Short PROM för Venous Insufficiency

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.

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Key information

Conditions

Superficial Venous Insufficiency Change After Treatment Quality of Life

Sex eligibility

All sexes

Study type

Observational

Primary location

Karlskoga venöst centrum, Karlskoga, Sweden

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Patient reported outcome measure

Other

2 questionnaires are tested against each other

Primary outcomes

the short PROM is valid for measurement of quality of life and detects change caused by treatment

Time frame: baseline and 8 weeks

Sponsors and collaborators

Lead sponsor

Karolinska Institutet

Other

Collaborators

Skandinaviska Forskningsstiftelsen för Åderbråck och andra Vensjukdomar

Registry information

Official study title

Validation of a Swedish Version of a Short Patient-Reported-Outcome-Measure for Superficial Venous Insufficiency

Important dates

Study start: 2018
Primary completion: 2019
Study completion: 2019
First posted: Mar 12, 2020
Registry last updated: Mar 12, 2020

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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