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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04184596
Other study ID # VF/1014/1070
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 11, 2020
Est. completion date August 31, 2020

Study information

Verified date February 2021
Source LinkCare GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to identify and weight attributes of topic and systemic pain treatment options relevant from the patients' perspective with peripheral neuropathic pain. The study will use a discrete choice experimental design to reach its objective.


Recruitment information / eligibility

Status Completed
Enrollment 153
Est. completion date August 31, 2020
Est. primary completion date July 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with diagnosed peripheral neuropathic pain (pNP) as assessed by study sites Exclusion Criteria: - Patients with no sufficient knowledge in written or oral German as assessed by study sites

Study Design


Intervention

Other:
Discrete Choice Experiment
An online-based Discrete-Choice Experiment (DCE) using a survey for stated treatment preferences and socio-demographics. Furthermore, the neuropathic pain component will be assessed in all patients with the Numeric Pain Rating Scale instrument.

Locations

Country Name City State
Germany LinkCare GmbH Stuttgart Baden-Württemberg
Germany Schmerz- und Palliativzentrum Rhein-Main Wiesbaden Hesse
Germany Schmerzpraxis Wiesbaden Wiesbaden Hesse

Sponsors (4)

Lead Sponsor Collaborator
LinkCare GmbH Grünenthal GmbH, Schmerz- und Palliativzentrum Rhein-Main Wiesbaden, Schmerzpraxis Wiesbaden

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Schubert T, Kern KU, Schneider S, Baron R. Oral or Topical Pain Therapy-How Would Patients Decide? A Discrete Choice Experiment in Patients with Peripheral Neuropathic Pain. Pain Pract. 2020 Dec 20. doi: 10.1111/papr.12989. [Epub ahead of print] — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Patient preferences for topical and systemic pain treatment attributes Utility values obtained via multinominal logit estimates from discrete choice experiment 20 minutes after survey start
Secondary Relevance of attributes attributed with topical and systemic pain treatment Derived from Likert scale 5 minutes after survey start
Secondary Marginal rate of substitution against pain reduction Derived from discrete choice experiment 20 minutes after survey start
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