Efficacy Study of a Facemask Device to Treat Hypotension
Primary Purpose
Hypotension
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Impedance Threshold Device
sham ITD
Sponsored by
About this trial
This is an interventional treatment trial for Hypotension focused on measuring hypotension, hypovolemia, dehydration, sepsis, blood loss
Eligibility Criteria
Inclusion Criteria: Conscious patient Systolic blood pressure < 95 mmHg Hypotension caused by blood loss, sepsis, or dehydration Exclusion Criteria: Hypotension secondary to heart failure Complaints of chest pain History of heart failure Complaints of shortness of breath
Sites / Locations
- Hennepin County Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Sham Comparator
Active Comparator
Arm Label
Sham ITD
active ITD
Arm Description
sham Impedance Threshold Device
active impedance threshold device
Outcomes
Primary Outcome Measures
Rise in Systolic Blood Pressure Over the First 10 Minutes of Use Compared to Baseline
Secondary Outcome Measures
Quantity of Fluid Administration
Full Information
NCT ID
NCT00256724
First Posted
November 18, 2005
Last Updated
July 24, 2013
Sponsor
Advanced Circulatory Systems
Collaborators
United States Department of Defense
1. Study Identification
Unique Protocol Identification Number
NCT00256724
Brief Title
Efficacy Study of a Facemask Device to Treat Hypotension
Official Title
Evaluation of an Inspiratory Impedance Threshold Device (ITD) in the Emergency Department for the Treatment of Hypotension
Study Type
Interventional
2. Study Status
Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
January 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Advanced Circulatory Systems
Collaborators
United States Department of Defense
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine if the impedance threshold device (ITD) attached to a facemask can increase blood pressure in patients who present to the emergency department with hypotension secondary to hypovolemia. The cause of hypovolemia could be blood loss, sepsis, or dehydration.
Detailed Description
The study is designed to test the hypothesis that use of the ITD will result in a rapid rise in blood pressure secondary to an increase in cardiac output. Either an active or sham ITD will be applied to hypotensive patients when initially presented to the emergency department with a systolic blood pressure of <95mmHg. The main endpoint of this study will be the rise in blood pressure over the first 10 minutes of use. Based upon pre-clinical studies as well as clinical studies performed to date, we hypothesize that use of the active ITD will result in a more rapid and higher blood pressure than the sham ITD. Multiple additional clinical parameters will also be compared between the two groups of patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension
Keywords
hypotension, hypovolemia, dehydration, sepsis, blood loss
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
47 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sham ITD
Arm Type
Sham Comparator
Arm Description
sham Impedance Threshold Device
Arm Title
active ITD
Arm Type
Active Comparator
Arm Description
active impedance threshold device
Intervention Type
Device
Intervention Name(s)
Impedance Threshold Device
Other Intervention Name(s)
ResQGard
Intervention Description
Active impedance threshold device
Intervention Type
Device
Intervention Name(s)
sham ITD
Intervention Description
sham impedance threshold device
Primary Outcome Measure Information:
Title
Rise in Systolic Blood Pressure Over the First 10 Minutes of Use Compared to Baseline
Time Frame
every 2 minutes during 10 minutes of device use
Secondary Outcome Measure Information:
Title
Quantity of Fluid Administration
Time Frame
during 10 minutes of device use
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Conscious patient
Systolic blood pressure < 95 mmHg
Hypotension caused by blood loss, sepsis, or dehydration
Exclusion Criteria:
Hypotension secondary to heart failure
Complaints of chest pain
History of heart failure
Complaints of shortness of breath
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keith Lurie, MD
Organizational Affiliation
Advanced Circulatory Systems
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hennepin County Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55404
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15828629
Citation
Convertino VA, Cooke WH, Lurie KG. Inspiratory resistance as a potential treatment for orthostatic intolerance and hemorrhagic shock. Aviat Space Environ Med. 2005 Apr;76(4):319-25.
Results Reference
background
PubMed Identifier
15864634
Citation
Convertino VA, Ratliff DA, Crissey J, Doerr DF, Idris AH, Lurie KG. Effects of inspiratory impedance on hemodynamic responses to a squat-stand test in human volunteers: implications for treatment of orthostatic hypotension. Eur J Appl Physiol. 2005 Jul;94(4):392-9. doi: 10.1007/s00421-005-1344-1. Epub 2005 Apr 28.
Results Reference
background
PubMed Identifier
15508665
Citation
Convertino VA, Ratliff DA, Ryan KL, Doerr DF, Ludwig DA, Muniz GW, Britton DL, Clah SD, Fernald KB, Ruiz AF, Lurie KG, Idris AH. Hemodynamics associated with breathing through an inspiratory impedance threshold device in human volunteers. Crit Care Med. 2004 Sep;32(9 Suppl):S381-6. doi: 10.1097/01.ccm.0000134348.69165.15.
Results Reference
background
PubMed Identifier
20634018
Citation
Smith SW, Parquette B, Lindstrom D, Metzger AK, Kopitzke J, Clinton J. An impedance threshold device increases blood pressure in hypotensive patients. J Emerg Med. 2011 Nov;41(5):549-58. doi: 10.1016/j.jemermed.2010.05.013. Epub 2010 Jul 15.
Results Reference
result
Links:
URL
http://www.advancedcirculatory.com
Description
Advanced Circulatory Systems, Inc. home page
Learn more about this trial
Efficacy Study of a Facemask Device to Treat Hypotension
We'll reach out to this number within 24 hrs