Central Venous Pressure Clinical Trial
Official title:
Clinical Validation of a Non-Invasive Central Venous Pressure Device in Comparison With Physical Examination in Patients With Chronic Kidney Disease and Healthy Volunteers
NCT number | NCT01243515 |
Other study ID # | MLS STP-9000006 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | November 17, 2010 |
Last updated | February 7, 2013 |
Verified date | February 2013 |
Source | Mespere Lifesciences Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Observational |
The primary objective of this study is to determine whether a correlation exists between the Mespere Non-Invasive Central Venous Pressure (NICVP) device for measuring central venous pressure (CVP), and assessment of CVP via physical examination.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 years or older at the time of enrolment - Chronic Kidney Disease patients and healthy volunteers - Participants should be able to provide written informed consent - Subject is termed eligible as determined by Pre-Screening Phase (as defined in protocol) Exclusion Criteria: - Unable to identify external jugular vein (EJV) - Unable to identify internal jugular vein (IJV) - Unable to access right side of subject's neck - Allergic to adhesive tape - History of central vein stenosis - Undergoing photodynamic therapy (PDT) - Presence of an arteriovenous fistula |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Canada | St. Joseph's Hamilton Healthcare | Hamilton | Ontario |
Lead Sponsor | Collaborator |
---|---|
Mespere Lifesciences Inc. | St. Joseph's Healthcare Hamilton |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Central Venous Pressure (CVP) | To determine if the CVP from the non-invasive monitor correlates with the CVP from physical examination | 0-3 hours | No |
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