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Qutenza TM in notalgia paresthtetica: pharmacoeconomic evaluation and patient acceptance with focus on intraepidermal C-fiber eradication

Qutenza TM in notalgia paresthtetica: pharmacoeconomic evaluation and patient acceptance with focus on intraepidermal C-fiber eradication

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00005189
Enrollment
100
Registered
2013-09-10
Start date
2014-05-01
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M79.29

Interventions

Group 1: Patients with Notalgia paraesthetica or brachioradial pruritus fill out several questionaires concerning clinical symptoms, quality of life and medical treatment regimens/costs and are treate

Sponsors

Astellas Pharma
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Diagnosis of notalgia paraesthetica or brachioradial pruritus with actual therapy need

Exclusion criteria

Exclusion criteria: Exclusion. 1. current and past (last 2 weeks) use of topical or systemic pain modulators (e.g., local anaesthetics in NP area, gabapentin, pregabalin), antidepressants (e.g., paroxetine, fluvoxamine, amitriptyline), antihistamines, topical or systemic steroids 2. diabetes, uncontrolled hypertension 3. history of skin disease or allergy likely to interfere with the study or known sensitivity to the test product or its ingredients, allergy to capsaicin 4. pregnancy, breast feeding 5. active psychosomatic and psychiatric diseases necessitating drug treatment 6. participation in any other research study during the previous 4 weeks. 7. previous participation in this study

Design outcomes

Primary

MeasureTime frame
Pharmacoeconomic and clinical evaluation of prescription patterns, symptoms, quality of life and nerve growth 3/6 months retrospectively and 3/6 months prospectively.

Countries

Germany

Contacts

Public ContactSabine Stoll

Hautklinik UKM

sabine.stoll@ukmuenster.der0251-8357470

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026