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NCT00253032 Clinical Trial

Pain Relief Investigation of NeuroModulation Therapy in Adult Humans

Chronic Musculoskeletal Pain Clinical Trial

Official title:
PRIMA Study: Pain Relief Investigation of NeuroModulation Therapy in an Adult Population: A Double Blind, Randomized, Multicenter, Placebo Controlled Trial.

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00253032
Other study ID # F05001
Secondary ID
Status Terminated
Phase Phase 3
First received November 11, 2005
Last updated March 2, 2006

Study information
Verified date March 2006
Source Fralex Therapeutics
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationCanada: Health Canada
Study type Interventional

Clinical Trial Summary

The study is being performed to determine the efficacy and safety of Fralex Neuromodulation Therapy (F-NMT), delivered by the Fralex PRIMA device, in reducing chronic musculoskeletal pain.

Recruitment information / eligibility

— Not specified —

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Device:
• PRIMA

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Fralex Therapeutics PharmaNet
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