Neuropathic Pain Database (NePDatabase)
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|ClinicalTrials.gov Identifier: NCT00669006|
Recruitment Status : Unknown
Verified March 2016 by Dwight Moulin, Lawson Health Research Institute.
Recruitment status was: Active, not recruiting
First Posted : April 29, 2008
Last Update Posted : March 22, 2016
To establish the infrastructure for a national neuropathic pain database.
To determine the longterm outcome of the management of chronic neuropathic pain including pain relief, disability, and quality of life.
|Condition or disease|
The database will provide standard information on demographics, diagnosis, treatment interventions and outcome modeled on guidelines from the expert panel on initiatives on Methods, Measurement and Pain Assessment in Clinical Trials (IMMPACT)(Turk et al.,Pain 2003;106:337-345) The IMMPACT panel determined that patients should be evaluated according to six core domains as follows: Pain, physical functioning, emotional functioning, subject rating of global satisfaction with treatment, symptoms and adverse events and subject disposition.
The database will allow us to examine outcomes based on single (eg. pregabalin) and multiple (e.g tricyclic antidepressants and gabalin) therapeutic interventions. Standard guidelines for management of neuropathic pain acknowledge that polypharmacy is appropriate when individual first line treatments fail to provide adequate pain relief (Gilron I et al., CMAJ 2006; 175: 265-275; Attal N et al., European Journal of Neurology 2006; 13: 1153-1169)
|Study Type :||Observational|
|Estimated Enrollment :||900 participants|
|Official Title:||National Neuropathic Pain Database Study|
|Study Start Date :||April 2008|
|Actual Primary Completion Date :||December 2012|
|Estimated Study Completion Date :||January 2017|
New patients with a diagnosis of Neuropathic Pain
- To establish the infrastructure for a national Neuropathic Pain Database. [ Time Frame: 2 years ]To establish the infrastructure for a National Neuropathic Pain Database, with a composite primary outcome measure in average pain intensity (based on average pain intensity of BPI) and reduction in disability (based on Interference Scale Score of BPI))
- To determine the longterm outcome of the management of chronic neuropathic pain including pain relief, disability and quality of life. [ Time Frame: 2 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00669006
|London Health Sciences Centre- St. Joseph's Health Care|
|London, Ontario, Canada, N6A 4V2|
|Principal Investigator:||Dwight Moulin, MD||London Health Sciences Centre- St. Joseph's Health Care|