Development and Validation for Taiwan Version ID Pain Questionnaire (ID Pain-T) and DN4 Questionnaire.
2 other identifiers
observational
325
0 countries
N/A
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2008
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 11, 2008
CompletedFirst Posted
Study publicly available on registry
January 24, 2008
CompletedStudy Start
First participant enrolled
March 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2008
CompletedJanuary 22, 2021
November 1, 2009
9 months
January 11, 2008
January 21, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Determine the optimal cut-off score of ID Pain-T Questionnaire for screening of neuropathic pain
end of study
Secondary Outcomes (2)
Evaluate the predictive power of ID Pain-T Questionnaire for diagnosis of neuropathic pain
end of study
Develop and evaluate validity of a short form diagnostic tool based on DN4 structure
end of study
Interventions
This is a non-interventional questionnaire validation study
Eligibility Criteria
patients of non-headache pain for more than 30 days and those whose age is more than 18 years old
You may qualify if:
- 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.
You may not qualify if:
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Pfizer CT.gov Call Center
Pfizer
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 11, 2008
First Posted
January 24, 2008
Study Start
March 1, 2008
Primary Completion
December 1, 2008
Study Completion
December 1, 2008
Last Updated
January 22, 2021
Record last verified: 2009-11