CClinicalTrials.gg
CompletedNCT01432652Updated Jul 29, 2015

The Efficacy of Aspirin in the Postoperative Period in Vascular Surgery

An observational study in Aspirin Resistance, sponsored by University of Lausanne Hospitals. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-07-29.

Sponsored by University of Lausanne Hospitals · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
45
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine the incidence of aspirin resistance in the population of vascular surgery patients; and to evaluate the changes in the efficacy of aspirin in the first five postoperative days.

Read the detailed description

About 15% of the general population shows resistance to the antiplatelet effects of aspirin, due to genetic polymorphisms and other factors. This resistance is a cause of increased myocardial infarction and death in patients undergoing percutaneous coronary interventions. Aspirin resistance can be detected by whole blood impedance aggregometry using the Multiplate® analyzer. The population of patients undergoing vascular surgery is at particular risk of suffering myocardial infarction in the perioperative period because of the high prevalence of risk factors. Most of these patients are treated by aspirin, as a measure of primary or secondary prevention. In this study we aim to establish baseline aspirin efficacy, as measured by the Multiplate® analyzer, in this high-risk population and evaluate the changes in aspirin efficacy over the first five days of the postoperative period. It is our hypothesis that the state of chronic inflammation, accompanying severe, generalized atherosclerosis results in a higher incidence of aspirin resistance in this population. Also, the surgical trauma and postoperative thrombocytosis may reduce the efficacy of aspirin in the postoperative period, partially explaining the increased incidence of postoperative myocardial infarction in this population.

In whole blood impedance aggregometry, the electrical impedance of the blood sample is measured by placing two electrodes in the recipient. After the addition of a platelet activator, the impedance will increase as platelets accumulate on the electrodes surfaces. Several activators, testing the patency of different platelet receptors can be used.

In this study, blood will be drawn on the day of surgery, and daily until the fifth postoperative day. Arachidonic acid, ADP, TRAP-6 and collagen will be used as activators. The first specifically tests the platelets reactivity to thromboxane A2. Aspirin inhibits this pathway, and the increase in impedance should therefore be limited in patients treated by this drug. The three other tests will be performed to evaluate the evolution of overall platelet reactivity in the postoperative period.

02

Conditions studied

  • Aspirin Resistance
03

In context

Lead sponsor

University of Lausanne Hospitals is the lead sponsor of 118 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Vascular surgery patients

Inclusion criteria

  • Patient undergoing peripheral vascular or abdominal aorta surgery.
  • Patient aged 18 years or older.
  • Patient treated by aspirin.

Exclusion criteria

Exclusion Criteria:

  • Incapacity to understand and consent to study.
  • Patient undergoing emergency surgery.
  • Patient treated by a cox-inhibitor other than aspirin.
  • Patient treated by omega-3-fatty acids.
  • Patient treated by ADP or GPIIb/IIIa receptor inhibitor.
  • Known coagulopathy, thrombopenia, thrombopathia or congenital or acquired thrombasthenia.
  • Terminal renal insufficiency.
  • Hepathic insufficiency.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
45 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • vascular surgery

    Patients undergoing vascular surgery

06

Study locations

1 site
  • University of Lausanne Hospitals
    Lausanne, Vaud 1011, Switzerland
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT01432652
Lead sponsor
University of Lausanne Hospitals
First posted
Sep 13, 2011
Start date
Sep 2011
Primary completion
Jan 2014
Completion
May 2014
Last update
Jul 29, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2011. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion