Blockade of Vascular Potassium Channels During Human Endotoxemia
Primary Purpose
Endotoxemia
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
endotoxin
Potassium channel blockers: TEA, Quinin, Tolbutamide
L-NMMA
Sponsored by
About this trial
This is an interventional treatment trial for Endotoxemia focused on measuring Endotoxemia, vascular potassium channels, cytokine, norepinephrine, regional blood flow,, inflammation,, ion channels,, nitric oxide synthase,, pharmacology.
Eligibility Criteria
Inclusion Criteria: healthy volunteers Exclusion Criteria: drug, alcohol, nicotine abuse
Sites / Locations
Outcomes
Primary Outcome Measures
Hemodynamics
Markers of Inflammation
Cytokines
Markers of Renal Injury
Inducible NO synthase expression
NO-metabolites
Mediators of Vascular reactivity
Sensitivity to norepinephrine
Secondary Outcome Measures
Full Information
NCT ID
NCT00185003
First Posted
September 13, 2005
Last Updated
October 16, 2008
Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT00185003
Brief Title
Blockade of Vascular Potassium Channels During Human Endotoxemia
Official Title
Blockade of Vascular Potassium Channels During Human Endotoxemia
Study Type
Interventional
2. Study Status
Record Verification Date
April 2008
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
June 2005 (Actual)
Study Completion Date
June 2005 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Activation of NO-synthase and vascular potassium (K) channels may play a role in the sepsis-induced attenuated sensitivity to norepinephrine. We examined whether various K channel blockers and NO-synthase inhibition could restore norepinephrine sensitivity during experimental human endotoxemia.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endotoxemia
Keywords
Endotoxemia, vascular potassium channels, cytokine, norepinephrine, regional blood flow,, inflammation,, ion channels,, nitric oxide synthase,, pharmacology.
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
endotoxin
Intervention Type
Drug
Intervention Name(s)
Potassium channel blockers: TEA, Quinin, Tolbutamide
Intervention Type
Drug
Intervention Name(s)
L-NMMA
Primary Outcome Measure Information:
Title
Hemodynamics
Time Frame
24 hrs after LPS administration
Title
Markers of Inflammation
Time Frame
24 hrs after LPS administration
Title
Cytokines
Time Frame
24 hrs after LPS administration
Title
Markers of Renal Injury
Time Frame
24 hrs after LPS administration
Title
Inducible NO synthase expression
Time Frame
24 hrs after LPS administration
Title
NO-metabolites
Time Frame
24 hrs after LPS administration
Title
Mediators of Vascular reactivity
Time Frame
24 hrs after LPS administration
Title
Sensitivity to norepinephrine
Time Frame
24 hrs after LPS administration
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
healthy volunteers
Exclusion Criteria:
drug, alcohol, nicotine abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Pickkers, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
16864730
Citation
Pickkers P, Dorresteijn MJ, Bouw MP, van der Hoeven JG, Smits P. In vivo evidence for nitric oxide-mediated calcium-activated potassium-channel activation during human endotoxemia. Circulation. 2006 Aug 1;114(5):414-21. doi: 10.1161/CIRCULATIONAHA.105.590232. Epub 2006 Jul 24.
Results Reference
result
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Blockade of Vascular Potassium Channels During Human Endotoxemia
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