Reliability of Myoton in Evaluating Skin Biomechanics in Breast Cancer-Related Lymphedema

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-80
SponsorKahramanmaras Sutcu Imam University

About this trial

This study aims to evaluate the intra- and inter-rater reliability of the MyotonPRO, a handheld device that measures the viscoelastic properties of the skin, in patients with breast cancer-related lymphedema. Twenty women with unilateral upper extremity lymphedema will be included. Each participant will undergo repeated skin assessments using the MyotonPRO by two independent raters. Additionally, ultrasonographic tissue characteristics and limb volume measurements will be performed. The findings are expected to contribute to the validation of the MyotonPRO for use in clinical lymphedema evaluation.

Eligibility criteria

Qualifiers

Female participants aged 18-80 years

Unilateral upper extremity lymphedema secondary to breast cancer surgery

Diagnosed with lymphedema at International Society of Lymphology (ISL) Stage 0, I, II, or III

Willing and able to provide informed consent

Disqualifiers

Bilateral upper extremity lymphedema

Cognitive or mental disorders that interfere with cooperation

Neurological diseases

Active infection

Trial design

Treatments tested in this trial

  • MyotonPRO

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

Kahramanmaras Sutcu Imam University

Lead sponsor

Fatih Sultan Mehmet Training and Research Hospital

Collaborator