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Kind and Duration of Possible Changes of the Sensory Profiles After the Topical Application of Capsaicin (8%) in Patients With Peripheral Neuropathic Pain
The treatment of neuropathic pain ist still a challenge. A new promising therapy is the use of capsaicin on skin. The investigators first experiences with capsaicin in patients with peripheral nerve injury showed changes in the sensibility, which achieved its maximal extent after four weeks and was regressive, but not completely abolished 1,5 months after application. In this study the investigators hope to specify, how long and in which way exactly this changes in sensibility appear.
The topical application of a high dosage of capsaicin (8%) is a new promising approach. There is only little knowledge about the extent and the duration of drug-induced changes of detection and pain thresholds based on a currently recommended standardized quantitative sensory testing (QST). The assessment of QST changes would be an important step forward to understand the way of action as well as the time course of the presumed recovering of the C-fiber function after topical application of a high concentration capsaicin patch. 10 patients suffering from peripheral neuropathic pain due to peripheral nerve injury and 10 patients suffering from postherpetic neuralgia will be investigated by QST following the protocol of DFNS (German Research Network on Neuropathic Pain), using both thermal and mechanical nociceptive as well as non-nociceptive stimuli. QST will be performed at the following times: * at baseline * 2, 4, 6, 8 weeks later, and every two weeks at least until re-occurrence of pain and/or recovering of the capsaicin-induced worsening of the C-fiber function.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Bergmannsheil, Department for pain management
Bochum, Germany
Start Date
April 1, 2011
Primary Completion Date
November 1, 2012
Completion Date
November 1, 2012
Last Updated
December 20, 2012
20
ACTUAL participants
quantitative sensory testing (QST)
PROCEDURE
Lead Sponsor
Ruhr University of Bochum
NCT02359825
NCT07000409
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06896994