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Does Acetylsalicylic Acid Reduce the Mortality of Patients Admitted to an Intensive Care Unit

Primary Purpose

Critical Illness

Status
Terminated
Phase
Phase 3
Locations
Austria
Study Type
Interventional
Intervention
Acetylsalicylic acid lysinate
0.9% sodium-chloride solution
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness focused on measuring acetylsalicylic acid, intensive care unit, mortality, Post mortem examination, bleeding

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients admitted to an intensive care unit
  • >18 years of age

Exclusion Criteria:

  • known allergy of intolerance to acetylsalicylic acid
  • recent surgery or planned surgery
  • active bleeding
  • known coagulation disorders
  • discretion of the physician
  • terminal illness (anticipated life expectancy <3months; e.g. due to cancer)
  • platelet count <20 000
  • recent ulcera
  • recent gastrointestinal bleeding
  • pregnancy

Sites / Locations

  • General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Acetylsalicylic acid lysinate

0.9% sodium-chloride solution

Arm Description

100mg Acetylsalicylic Acid

0.9% sodium-chloride solution

Outcomes

Primary Outcome Measures

28-day Mortality
Standard outcome measure of investigational intensive care unit trials.

Secondary Outcome Measures

Intensive Care Unit Mortality
Mortality of patients during their intensive care unit stay, 90 day mortality, potentially longer
Number of Patients Who Developed a Thrombotic or Embolic Complications During the Trial
clinically relevant thromboembolic events assessed by standard care, potentially longer
Bleeding Incidences
all bleeding incidence during the intensive care unit stay will be recorded. major bleeding criteria are taken from the Thrombolysis in myocardial infarction study (TIMI-Triton-38), potentially longer

Full Information

First Posted
October 24, 2012
Last Updated
November 28, 2019
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT02285153
Brief Title
Does Acetylsalicylic Acid Reduce the Mortality of Patients Admitted to an Intensive Care Unit
Official Title
Does Acetylsalicylic Acid Reduce the Mortality of Patients Admitted to an Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Terminated
Why Stopped
Recruitment of planned number of Subjects was not feasible.
Study Start Date
November 15, 2011 (Actual)
Primary Completion Date
September 5, 2017 (Actual)
Study Completion Date
November 10, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Platelets play a central part not just in homeostasis and thrombosis as the primary effector cells, but they are also key cells in the regulation of the immunological response to various stressors. After activation, platelets release their granules which store different inflammatory mediators that induce coagulation, recruit further platelets, activate complement, attract neutrophils and leukocytes and regulate the vascular tone. Platelets activated by systemic inflammation and infection, may also contribute to the development of multiple organ failure. Thus, inhibition of platelet activation may have beneficial effects on critically ill patients. the investigators hypothesize that acetylsalicylic acid reduces the mortality of medical intensive care unit patients. In a retrospective study acetylsalicylic acid use was associated with a substantial reduction in a medical intensive care unit population (Winning et al., 2010). The investigators will conduct a randomized, double-blind study including 460 patients (2x230), who will be randomized to receive 100mg acetylsalicylic acid(daily, intravenous) or a placebo (0,9% sodium-choride solution) to assess whether acetylsalicylic acid reduces the mortality of medical intensive care unit patients. Main outcome criteria will be 28/90day-mortality. Furthermore the investigators will assess whether acetylsalicylic acid reduces the risk of suffering thromboembolic complications. Post-mortem examinations will be conducted in all patients who die in the course of the study. Furthermore we will assess bleeding rates, intensive care unit mortality and pharmacokinetic and pharmacodynamic properties of acetylsalicylic acid in the intensive care unit population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness
Keywords
acetylsalicylic acid, intensive care unit, mortality, Post mortem examination, bleeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
double blind
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acetylsalicylic acid lysinate
Arm Type
Experimental
Arm Description
100mg Acetylsalicylic Acid
Arm Title
0.9% sodium-chloride solution
Arm Type
Placebo Comparator
Arm Description
0.9% sodium-chloride solution
Intervention Type
Drug
Intervention Name(s)
Acetylsalicylic acid lysinate
Intervention Description
100mg intravenously administered Acetylsalicylic Acid lysinate per day
Intervention Type
Drug
Intervention Name(s)
0.9% sodium-chloride solution
Intervention Description
Placebo, intravenously administered, daily
Primary Outcome Measure Information:
Title
28-day Mortality
Description
Standard outcome measure of investigational intensive care unit trials.
Time Frame
28-days
Secondary Outcome Measure Information:
Title
Intensive Care Unit Mortality
Description
Mortality of patients during their intensive care unit stay, 90 day mortality, potentially longer
Time Frame
up to 90 days after inclusion
Title
Number of Patients Who Developed a Thrombotic or Embolic Complications During the Trial
Description
clinically relevant thromboembolic events assessed by standard care, potentially longer
Time Frame
average 28 days
Title
Bleeding Incidences
Description
all bleeding incidence during the intensive care unit stay will be recorded. major bleeding criteria are taken from the Thrombolysis in myocardial infarction study (TIMI-Triton-38), potentially longer
Time Frame
average 28days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients admitted to an intensive care unit >18 years of age Exclusion Criteria: known allergy of intolerance to acetylsalicylic acid recent surgery or planned surgery active bleeding known coagulation disorders discretion of the physician terminal illness (anticipated life expectancy <3months; e.g. due to cancer) platelet count <20 000 recent ulcera recent gastrointestinal bleeding pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernd Jilma, Ao. Univ.-Prof. Dr. med
Organizational Affiliation
Medical University of Vienna, Department of Clinical Pharmacology
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Hospital
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

Citations:
PubMed Identifier
19770746
Citation
Winning J, Neumann J, Kohl M, Claus RA, Reinhart K, Bauer M, Losche W. Antiplatelet drugs and outcome in mixed admissions to an intensive care unit. Crit Care Med. 2010 Jan;38(1):32-7. doi: 10.1097/CCM.0b013e3181b4275c.
Results Reference
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Does Acetylsalicylic Acid Reduce the Mortality of Patients Admitted to an Intensive Care Unit

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