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NCT00167726 Clinical Trial

Neuraxial and Neurolytic Analgesia for Intractable Pain

Pain Clinical Trial

Official title:
Neuraxial and Neurolytic Analgesia for Intractable Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00167726
Other study ID # 2004-0482
Secondary ID
Status Completed
Phase N/A
First received September 9, 2005
Last updated December 5, 2014
Start date January 2005
Est. completion date June 2011

Study information
Verified date December 2014
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to collect longitudinal data on outcomes of neuraxial or neurolytic procedures in patients with intractable cancer and chronic noncancer pain so that we may contribute to the growing evidence for or against these therapies and to provide data for ongoing quality improvement activities.

Recruitment information / eligibility
Status Completed
Enrollment 19
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- treated for intractable pain by the UW Interventional Pain Treatment program

- inpatient or outpatient

Exclusion Criteria:

- less than 18 years of age

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Wisconsin Madison Wisconsin

Sponsors (1)
Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prospective review of pain The purpose of this study was to collect longitudinal data on outcomes of neuraxial or neurolytic procedures in patients with intractable cancer and chronic noncancer pain so that we may contribute to the growing evidence for or against these therapies and to provide data for ongoing quality improvement activities. six years No
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