Viewing Study NCT00253032



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Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00253032
Status: TERMINATED
Last Update Posted: 2006-03-03
First Post: 2005-11-11

Brief Title: Pain Relief Investigation of NeuroModulation Therapy in Adult Humans
Sponsor: Fralex Therapeutics
Organization: Fralex Therapeutics

Study Overview

Official Title: PRIMA Study Pain Relief Investigation of NeuroModulation Therapy in an Adult Population A Double Blind Randomized Multicenter Placebo Controlled Trial
Status: TERMINATED
Status Verified Date: 2006-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None