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NCT00130130 Clinical Trial

Testing the Effects of an Algorithm for Neuropathic Pain on Patient and System Outcomes

Pain Clinical Trial

Official title:
Testing the Effects of an Algorithm for Neuropathic Pain on Patient and System Outcomes

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00130130
Other study ID # D 0403
Secondary ID ONS
Status Completed
Phase Phase 1/Phase 2
First received August 12, 2005
Last updated January 30, 2012
Start date August 2005
Est. completion date December 2011

Study information
Verified date January 2012
Source Dartmouth-Hitchcock Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The overall purpose of this project is to improve nurse skills regarding neuropathic pain (NP) assessment, treatment and referral practices through implementation of an evidence-based algorithm and to improve selected patient outcomes as a result of algorithm use.

Description:

Neuropathic pain (NP) is defined as pain that arises from injury, disease or dysfunction of the central or peripheral nervous system. For the patient focused phase of the project NP treatment will be guided via the Peripheral Neuropathy Treatment Algorithm. Patients will receive algorithm-specific treatment for 12 weeks.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date December 2011
Est. primary completion date September 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Cancer patients experiencing NP from a variety of causes

- NP Visual Analogue Scale (VAS) score equal to or > 4 with 12 week estimated duration

- Karnofsky Performance Status (KPS) 60% or greater

- Age greater than 18

Exclusion Criteria:

- Patients undergoing anticancer or invasive pain procedures specifically intended to palliate NP are ineligible

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Dartmouth Hitchcock Medical Center Lebanon New Hampshire

Sponsors (1)
Lead Sponsor Collaborator
Dartmouth-Hitchcock Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary To implement an evidence based screening, assessment, treatment, and referral guideline for hematology/oncology patients with NP receiving care outcome measures will consist of the NPVAS, and a PPCPS adapted rom the original project. Adequate satisfaction will be defined as 25% or mor of all patients reporting being very or completely satisfied as measured by PPCPS No
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