SBIR-STTR Award

Neuromodulation For Stroke Shoulder Pain
Award last edited on: 1/29/14

Sponsored Program
SBIR
Awarding Agency
NIH : NINDS
Total Award Amount
$303,701
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Maria Elaine Bennett

Company Information

NDI Medical LLC (AKA: Neurostim Design and Innovation~NDI)

22901 Millcreek Boulevard Suite 110
Cleveland, OH 44122
   (216) 378-9106
   info@ndimedical.com
   www.ndimedical.com
Location: Multiple
Congr. District: 11
County: Cuyahoga

Phase I

Contract Number: 1R43NS066524-01A1
Start Date: 8/5/10    Completed: 7/31/11
Phase I year
2010
Phase I Amount
$303,701
Shoulder pain is a common complication following stroke. A prospective population-based study on first-time stroke patients found that almost one third of patients developed shoulder pain, most describing their pain as moderate to severe. The treatment of shoulder pain is a crucial step towards recovery for stroke survivors. Shoulder pain has been found to lengthen the time to recovery, produce insomnia, and require additional medications or interventions during rehabilitation. The primary objective of this Phase I project is to determine the feasibility of a novel treatment for post-stroke shoulder pain using percutaneous intramuscular electrical stimulation. The first specific aim of this project is to determine the feasibility of the approach. The second specific aim is to evaluate the effect of percutaneous intramuscular electrical stimulation on shoulder pain intensity. The feasibility of reducing pain with intramuscular electrical stimulation will be assessed through the administration of a validated pain questionnaire. Endpoints will be measured at baseline, during and directly following the sham period, and during and directly following the treatment period. A multi-center randomized clinical trial will be executed in a Phase II project. The results of this randomized trial will be used to design a larger pivotal study that will be used to support an FDA pre-market approval (PMA) application for product commercialization. Our long-term objective is to develop a safe and effective neuromodulation treatment for patients with post-stroke shoulder pain. ,

Public Health Relevance:
Each year in the United States, almost one third of the 695,000 new stroke survivors develop shoulder pain, most describing their pain as moderate to severe. The treatment of shoulder pain is an important step towards recovery for stroke survivors, as shoulder pain has been found to interfere with therapeutic exercises, lengthen the time to recovery, produce insomnia, and require additional medications or interventions during rehabilitation. We propose to develop a novel therapy that uses electrical stimulation to treat post-stroke shoulder pain.

Thesaurus Terms:
21+ Years Old;Adopted;Adult;Affect;American Heart Association;Apoplexy;Armpit;Axilla;Axillary;Bandage;Brief Pain Inventory;Cerebral Stroke;Cerebrovascular Apoplexy;Cerebrovascular Stroke;Cerebrovascular Accident;Clinical;Communities;Complex;Complication;Cutaneous;Data;Deltoid;Drugs;Electric Stimulation;Electrical Stimulation;Electrodes;Enrollment;Exercise;Exercise, Physical;Feasibility Studies;Head;Human, Adult;Implant;Insomnia;Insomnia Disorder;Intervention;Intervention Strategies;Intramuscular;Lead;Left;Location;Marketing;Measures;Medication;Methods;Motor;Multi-Institutional Clinical Trial;Multi-Center Clinical Study;Multi-Center Clinical Trial;Multi-Site Clinical Study;Multi-Site Clinical Trial;Muscle;Muscle Cell Contraction;Muscle Contraction;Muscle Fatigue;Muscle Tissue;Muscular Contraction;Muscular Fatigue;Nerve;Nervous;Pain;Painful;Participant;Patient Care;Patient Care Delivery;Patients;Pb Element;Pharmaceutic Preparations;Pharmaceutical Preparations;Phase;Physical Health Services / Rehabilitation;Physicians;Physiologic Pulse;Placebo Effect;Population;Prevalence;Procedures;Pulse;Questionnaires;Randomized;Randomized Clinical Trials;Recovery;Rehabilitation;Rehabilitation Therapy;Rehabilitation, Medical;Reporting;Safety;Shoulder;Shoulder Pain;Site;Sleeplessness;Staging;Staging System;Stimulus;Stroke;Structure Of Deltoid Muscle;Study Section;Surface;Survivors;System;System, Loinc Axis 4;Testing;Therapeutic;Time;Treatment Period;Underarm;United States;Vascular Accident, Brain;Visual;Adult Human (21+);Arm;Base;Brain Attack;Cerebral Vascular Accident;Clinical Efficacy;Clinical Significance;Clinically Significant;Commercialization;Cost;Deltoid Muscle Structure;Design;Designing;Drug/Agent;Effective Therapy;Enroll;Expectancy Effect;Expectation Effect;Heavy Metal Pb;Heavy Metal Lead;Improved;Interventional Strategy;Multi Center Clinical Study;Multi Center Clinical Trial;Multi Site Clinical Study;Multi Site Clinical Trial;Neural Control;Neural Regulation;Neuroregulation;Nocebo;Novel;Placebo Response;Population Based;Post Stroke;Poststroke;Prevent;Preventing;Prospective;Public Health Relevance;Randomisation;Randomization;Randomized Trial;Randomly Assigned;Rehabilitative;Stroke;Stroke Recovery;Success;Treatment Days;Treatment Duration

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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