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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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