The objective of this study is to assess the efficacy and safety of twice daily oral difelikefalin for the treatment of adult participants with Pruritus (itch) associated with Notalgia Paresthetica (N.P.).
Volunteers needed for a 15 week long clinical trial with up to 7 office visits for an investigational product. Up to $2,410.00 stipend available.
To Qualify, you must meet the following INCLUSION CRITERIA:
1.) 18 to 80 Years of Age
2.) Current Notalgia Paresthetica
3.) Moderate to Severe condition (to be assessed at your in office screening visit)
To Qualify, you must NOT meet the following EXCLUSION CRITERIA:
1.) Itch (pruritus) caused by something other than N.P.
2.) Unwilling to discontinue current Notalgia Paresthetica treatments
3.) Female who is pregnant or breastfeeding
ClinicalTrials.gov Identifier: NCT 05978063
https://clinicaltrials.gov/study/NCT05978063?term=cara&intr=notalgia%20paresthetica&rank=2
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