The aim of this study is to monitor the effectiveness and used dosage of the 8% capsaicin patch in real-life clinical practice in the treatment of post-operative neuropathic pain.
Study Type
OBSERVATIONAL
Enrollment
319
capsaicin patch
Site CZ42019 Hospital
Benešov, Czechia
Percentage rate of responders
at least 30% decrease in pain intensity as compared to the baseline
Time frame: Baseline, Week 13
Basic demographic parameters
age, gender, history of the disease, other diagnoses
Time frame: Baseline
Previous treatment of neuropathy
type of treatment, dosage, combination, treatment line number
Time frame: Baseline
Reason for a change in the therapy
Time frame: Baseline
Dose
number of patches, area of application and frequency of treatment with 8% capsaicin
Time frame: Baseline, Week 13 and Week 26
Size of the area affected by neuropathic pain
Time frame: Baseline, Week 13 and Week 26
Concomitant neuropathic medication
Time frame: Baseline, Week 13 and Week 26
Efficacy of treatment
changes in NPRS score between weeks 0 and week 8, week 13 and week 26
Time frame: Baseline, Week 8, Week 13 and Week 26
Quality of life questionnaire (EQ-5D)
Time frame: Baseline, Week 8, Week 13 and Week 26
Consumption of rescue analgesic medication
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Site CZ42026 Hospital
Beroun, Czechia
Site CZ42008 Onco Clinic
Brno, Czechia
Site CZ42001 Sv. Anna Hospital
Brno, Czechia
Site CZ42007 Private Practice
České Budějovice, Czechia
Site CZ42015 Hospital
Havlíčkův Brod, Czechia
Site CZ42029 Hospital
Hořovice, Czechia
Site CZ42009 University Hospital
Hradec Králové, Czechia
Site CZ42004 Hospital
Jihlava, Czechia
Site CZ42022 Hospital
Karlovy Vary, Czechia
...and 19 more locations
Time frame: Baseline, Week 8, Week 13 and Week 26
Consumption of additional medical care for neuropathic pain
extra visits, hospitalisation
Time frame: Baseline, Week 8, Week 13 and Week 26