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NCT00599768 Clinical Trial

Development and Validation for Taiwan Version ID Pain Questionnaire (ID Pain-T) and DN4 Questionnaire.

Neuropathic Pain Clinical Trial

Official title:
Development and Validation for Taiwan Version ID Pain Questionnaire (ID Pain-T) and DN4 Questionnaire.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00599768
Other study ID # A0081175
Secondary ID TWN-2006-CNS-001
Status Completed
Phase
First received
Last updated
Start date March 2008
Est. completion date December 2008

Study information
Verified date November 2009
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This prospective cohort and multi-site study aims to develop Taiwan version (ID Pain-T) based on the original versions of ID Pain and also DN4, and validate both ID Pain-T and DN4 applied in Taiwanese subjects at the clinical setting.

Recruitment information / eligibility
Status Completed
Enrollment 325
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Subjects without headache pain over 30 days and at least 18 years old who will visit the clinic, inclusive of male and female. - Subjects who are able to complete the ID Pain-T Questionnaire. Exclusion Criteria: - Subjects who are illiterate or unable to complete questionnaire. - Subjects who are currently participating in another study or have participated in another pain study within one month of study entry. - Subjects with low back pain are unable to participate in this study; as the sciatica caused by the piriformis (exclusive of the other types of sciatic pain), lumbago, unclear identification in nerve injury (e.g. complex regional pain syndrome type I) or mixed origin (e.g. cancer pain).

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• ID-Pain DN4 Questionnaire
This is a non-interventional questionnaire validation study

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Outcome
Type Measure Description Time frame Safety issue
Primary Determine the optimal cut-off score of ID Pain-T Questionnaire for screening of neuropathic pain end of study
Secondary Evaluate the predictive power of ID Pain-T Questionnaire for diagnosis of neuropathic pain end of study
Secondary Develop and evaluate validity of a short form diagnostic tool based on DN4 structure end of study
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