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Survey of a representative sample of patients after topicala) capsaicin 8% therapyb) lidocaine 5% therapyc) botulinum toxin A injectio

Conditions
Patients treated with at least one of the capsaicin, lidocaine or botulinum toxin at least once
Registration Number
DRKS00011877
Lead Sponsor
Berufgenossenschaftliches Universitätsklinikum Bergmannsheil gGmbH, Abteilung für Schmerzmedizin
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
224
Inclusion Criteria

All patients who a) received at least one treatment with the topical capsaicin 8% (Qutenza ®) in the own clinic since 2010 b) since 2008 received at least one Versatis® therapy in the own clinic c) since 2014 received at least one Botox® injection in the own clinic

Exclusion Criteria

lack of ability to provide information, cognitive limitations

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
overview of the frequency / reasons for a possible discontinuation of therapy or the frequency / reasons for further treatment
Secondary Outcome Measures
NameTimeMethod
Assessment of effectiveness (global impression)
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