The aim of the LedRad LTE study is to determine the current complaints, late side effects and satisfaction of patients who were treated with radiotherapy for Ledderhose disease at least two years ago.
Study Type
OBSERVATIONAL
Enrollment
68
Patients who received a total dose of 30 Gy
University Medical Center Groningen
Groningen, Netherlands
Current pain
Determine pain with the numeric rating scale. A 11-point pain scale ranging from 0=no pain to 10=worst pain
Time frame: at least 2 years after treatment
Worst pain
Determine pain with the numeric rating scale. A 11-point pain scale ranging from 0=no pain to 10=worst pain
Time frame: at least 2 years after treatment
Quality of Life
Assess the impact on quality of life of the treatment with radiotherapy for this study population with the EURO-Qol-5D-5L
Time frame: at least 2 years after treatment
Late side effects of treatment
Is treatment still effective and/or are there any (unknown) side effects of treatment
Time frame: at least 2 years after treatment
Satisfaction with radiotherapy treatment for Ledderhose disease
Determine patient satisfaction with the radiotherapy treatment for Ledderhose disease using a self developed questionnaire
Time frame: at least 2 years after treatment
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