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The Effects of Oral Dipyridamole Treatment on the Innate Immune Response During Human Endotoxemia

Primary Purpose

Endotoxemia

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Dipyridamole
Placebo
LPS
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Endotoxemia focused on measuring Adenosine, Endotoxin, Innate Immunity, Dipyridamole

Eligibility Criteria

18 Years - 35 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥ 18 and ≤ 35 years
  • Male
  • Healthy

Exclusion Criteria:

  • Use of any medication.
  • History of allergic reaction to dipyridamole
  • Bleeding disorder.
  • Smoking.
  • Previous spontaneous vagal collapse.
  • History, signs or symptoms of cardiovascular disease.
  • Cardiac conduction abnormalities on the ECG consisting of a 2nd degree atrioventricular block or a complex bundle branch block.
  • Hypertension (defined as RR systolic > 160 or RR diastolic > 90).
  • Hypotension (defined as RR systolic < 100 or RR diastolic < 50).
  • Renal impairment (defined as plasma creatinin >120 μmol/l).
  • Liver enzyme abnormalities or positive hepatitis serology.
  • Positive HIV serology or any other obvious disease associated with immune deficiency.
  • Febrile illness in the week before the LPS challenge.
  • Participation in another drug trial or donation of blood 3 months prior to the planned LPS challenge.

Sites / Locations

  • Radboud University Nijmegen Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Endotoxemia placebo

Endotoxemia Dipyridamole

Arm Description

Endotoxin combined with placebo

Endotoxin combined with Dipyridamol treatment

Outcomes

Primary Outcome Measures

Circulating cytokines
TNFx, IL6, IL10, IL1RA

Secondary Outcome Measures

Hemodynamics
Continious heart rate and blood pressure measurement
Sensitivity to norepinephrine
Venous occlusion plethysmography
Endothelial-dependent and independent vasorelaxation
Venous occlusion plethysmography
Markers of endothelial damage and circulating endothelial cells
circulating adhesion molecules (ICAM, VCAM, E-selectin, P-selectin) circulating endothelial cells
Urinary excretion of markers of renal injury
GSTAlpha1-1 and GSTPi1-1
Adenosine and related nucleotide concentrations
Additional blood samples will be drawn for genetic testing and measurement of: mRNA and proteins part of the adenosine metabolism
Oxydative stress
Thiols, neutrophilic burst, calcium release of neuthrophils, TBARS, Carbonyls, FRAP, Myeloperoxidase, catalase, Griess assay

Full Information

First Posted
March 18, 2010
Last Updated
November 4, 2010
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01091571
Brief Title
The Effects of Oral Dipyridamole Treatment on the Innate Immune Response During Human Endotoxemia
Official Title
The Effects of Oral Dipyridamole Treatment on the Innate Immune Response During Human Endotoxemia.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Radboud University Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
During sepsis and septic shock the immune response can be overwhelming leading to excessive tissue damage, organ failure and death. Ideally, the inflammatory response is modulated leading to both adequate protection to invading pathogens as well as limitation of an exuberant immune response. In the last few years adenosine is proposed to have a central role in the modulation of inflammation. In unfavorable conditions such as hypoxia, ischemia or inflammation adenosine is quickly up-regulated; with concentrations up to tenfold in septic patients. Many animal studies have shown that adenosine is able to attenuate the inflammatory response and decrease mortality rates. Therefore, pharmacological elevation of the adenosine concentration is an potential target to attenuate inflammation and limit organ injury. Dipyridamole, an adenosine re-uptake inhibitor is able to increase the adenosine concentration and limit ischemia-reperfusion injury. In order to study the effects of dipyridamole on the inflammatory response we aim to use the so called human endotoxemia model. This model permits elucidation of key players in the immune response to a gram negative stimulus in vivo, therefore serving as a useful tool to investigate potential novel therapeutic strategies in a standardized setting.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endotoxemia
Keywords
Adenosine, Endotoxin, Innate Immunity, Dipyridamole

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Endotoxemia placebo
Arm Type
Placebo Comparator
Arm Description
Endotoxin combined with placebo
Arm Title
Endotoxemia Dipyridamole
Arm Type
Experimental
Arm Description
Endotoxin combined with Dipyridamol treatment
Intervention Type
Drug
Intervention Name(s)
Dipyridamole
Other Intervention Name(s)
Persantin retard
Intervention Description
Oral treatment with dipyridamole 200 mg twice daily during seven consecutive days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo twice daily during seven consecutive days
Intervention Type
Other
Intervention Name(s)
LPS
Other Intervention Name(s)
Human endotoxemia
Intervention Description
The LPS derived from E. coli O:113 2ng/kg iv will be injected in 1 minute at a dosage of 2 ng/kg body weight.
Primary Outcome Measure Information:
Title
Circulating cytokines
Description
TNFx, IL6, IL10, IL1RA
Time Frame
24 hours after LPS administration
Secondary Outcome Measure Information:
Title
Hemodynamics
Description
Continious heart rate and blood pressure measurement
Time Frame
24 hours after LPS administration
Title
Sensitivity to norepinephrine
Description
Venous occlusion plethysmography
Time Frame
24 hrs after LPS administration
Title
Endothelial-dependent and independent vasorelaxation
Description
Venous occlusion plethysmography
Time Frame
24 hours after LPS administration
Title
Markers of endothelial damage and circulating endothelial cells
Description
circulating adhesion molecules (ICAM, VCAM, E-selectin, P-selectin) circulating endothelial cells
Time Frame
24 hrs after LPS administration
Title
Urinary excretion of markers of renal injury
Description
GSTAlpha1-1 and GSTPi1-1
Time Frame
24 hrs after LPS administration
Title
Adenosine and related nucleotide concentrations
Time Frame
24 hrs after LPS administration
Title
Additional blood samples will be drawn for genetic testing and measurement of: mRNA and proteins part of the adenosine metabolism
Time Frame
24 hours after LPS administration
Title
Oxydative stress
Description
Thiols, neutrophilic burst, calcium release of neuthrophils, TBARS, Carbonyls, FRAP, Myeloperoxidase, catalase, Griess assay
Time Frame
24 hours after LPS administration

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 and ≤ 35 years Male Healthy Exclusion Criteria: Use of any medication. History of allergic reaction to dipyridamole Bleeding disorder. Smoking. Previous spontaneous vagal collapse. History, signs or symptoms of cardiovascular disease. Cardiac conduction abnormalities on the ECG consisting of a 2nd degree atrioventricular block or a complex bundle branch block. Hypertension (defined as RR systolic > 160 or RR diastolic > 90). Hypotension (defined as RR systolic < 100 or RR diastolic < 50). Renal impairment (defined as plasma creatinin >120 μmol/l). Liver enzyme abnormalities or positive hepatitis serology. Positive HIV serology or any other obvious disease associated with immune deficiency. Febrile illness in the week before the LPS challenge. Participation in another drug trial or donation of blood 3 months prior to the planned LPS challenge.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bart P Ramakers, MD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Centre
City
Nijmegen
ZIP/Postal Code
6500 HB
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
22129171
Citation
Ramakers BP, Riksen NP, Stal TH, Heemskerk S, van den Broek P, Peters WH, van der Hoeven JG, Smits P, Pickkers P. Dipyridamole augments the antiinflammatory response during human endotoxemia. Crit Care. 2011;15(6):R289. doi: 10.1186/cc10576. Epub 2011 Nov 30.
Results Reference
derived

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The Effects of Oral Dipyridamole Treatment on the Innate Immune Response During Human Endotoxemia

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