Viewing Study NCT02468934



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Study NCT ID: NCT02468934
Status: COMPLETED
Last Update Posted: 2018-09-04
First Post: 2015-04-22

Brief Title: Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty TKA Using the SPRINT System
Sponsor: SPR Therapeutics Inc
Organization: SPR Therapeutics Inc

Study Overview

Official Title: A Prospective Case Series Study of SPR Peripheral Nerve Stimulation PNS Therapy for the Treatment of Pain Following Total Knee Arthroplasty TKA Utilizing Preoperative Lead Placement
Status: COMPLETED
Status Verified Date: 2018-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine if electrical stimulation small levels of electricity can safely and effectively reduce pain following total knee replacement or total knee arthroplasty TKA This study involves a device called the SPRINT System The SPRINT System delivers mild electrical stimulation to nerves in the leg that received the knee replacement The SPRINT System includes a small wire called a lead that is placed through the skin in the upper leg It also includes a device worn on the body that delivers stimulation called the SPRINT Stimulator
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