Spinal Cord Injuries Clinical Trial
Official title:
Functional Electrical Stimulation for Production of Artificial Cough
NCT number | NCT00589199 |
Other study ID # | IRB93-00133 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 1993 |
Est. completion date | January 2010 |
Verified date | July 2019 |
Source | MetroHealth Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the present study is to assess the utility of abdominal muscle stimulation to provide large positive airway pressures and expiratory airflow thus simulating cough. Restoration of cough in spinal cord injured patients may reduce the incidence of respiratory complications such as atelectasis, respiratory tract infections and respiratory failure.
Status | Completed |
Enrollment | 5 |
Est. completion date | January 2010 |
Est. primary completion date | January 2010 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patients with cervical or thoracic spinal cord injury Exclusion Criteria: - Significant cardiovascular disease - Active lung disease - Pacemaker or other metallic implant - Legally incompetent |
Country | Name | City | State |
---|---|---|---|
United States | MetroHealth Medical Center | Cleveland | Ohio |
Lead Sponsor | Collaborator |
---|---|
MetroHealth Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measurements of airway pressure and expiratory flow rate to evaluate efficacy of cough | one year | ||
Secondary | Incidence of respiratory complications | one year |
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