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Transcranial Doppler (TCD) Assessment During Early Anti-thrombotic Therapy After Bioprosthetic Aortic Valve Replacement

"Transcranial Doppler Assessment of Cerebral Embolization During Early Anti-thrombotic Therapy After Bioprosthetic Aortic Valve Replacement: Comparison of High-dose Aspirin Versus Warfarin Plus Low-dose Aspirin"

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00465218
Acronym
Tissue-Valve
Enrollment
70
Registered
2007-04-24
Start date
2007-03-01
Completion date
2011-03-01
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Valve Disease

Keywords

Bioprosthesis, Thrombosis, Cerebral emboli, Transcranial Doppler, Platelet function tests

Brief summary

The purpose of this study is to determine if there is any difference in the counts of cerebral emboli and platelet function between two prophylactic treatments of thrombosis currently used at University of Ottawa Heart Institute for the first three months after surgery in low-risk patients undergoing aortic valve replacement with a bioprosthetic valve: 1) daily use of high-dose aspirin \[325 mgs\], and 2) the combination of oral Warfarin \[target INR 2.0 to 3.0\] and low-dose aspirin \[81 mg\].

Detailed description

Background: There are several medications used to prevent blood clotting in patients undergoing surgical replacement of their aortic valves with tissue valves. One of these medications is called warfarin (Coumadin ®) which prevents blood clotting by making the blood "thinner." Another medication is aspirin which prevents the aggregation (clustering) of cells in the blood called platelets. Some clinicians consider that using only aspirin should be enough to protect the patients against the presence of clots in the blood, but others consider that aspirin should be combined with warfarin for better protection. Moreover, physicians express concern over the use of oral anticoagulation due to the possibility of an increased risk of bleeding. The effects of these medications for preventing blood clots traveling to the brain after the surgery are currently unknown. Transcranial doppler ultrasound will be used in these patients to evaluate non-invasively the quantity of fragments of clots circulating in the arteries of the brain. In addition, platelet function will be measured to determine how effective these treatments are for preventing the aggregation of the blood cells called platelets, which may be involved in clot formation. Objective: Our purpose is to determine if there is any difference in the counts of cerebral emboli and platelet function between two prophylactic treatments of thrombosis currently used in our institution for the first three months after surgery in these patients: 1) daily use of high-dose aspirin \[325 mgs\], and 2) the combination of oral Warfarin \[target INR 2.0 to 3.0\] and low-dose aspirin \[81 mg\]. Methods: Patients with low risk profile undergoing primary aortic valve replacement with a bioprosthetic (tissue) valve will be eligible for the study. Patients will receive one of the two prophylactic treatments of thrombosis (1 or 2) depending on the surgeon's preference. Platelet function will be measured before surgery and transcranial doppler within the first 24 hours immediately after the surgery. At the end of one month following surgery, all patients will undergo transcranial doppler and platelet function assessment. The study will be powered on demonstrating the hypothesis of substantial equivalence between the two treatments as regarding the primary outcome (cerebral emboli). Outcome measures: 1. Primary outcome: Bilateral counts of cerebral emboli in the middle cerebral arteries with transcranial doppler ultrasound at one month after surgery 2. Secondary outcomes: Platelet function, incidence of major adverse neurologic and bleeding events at one month following surgery

Interventions

PROCEDUREProphylaxis of Thrombosis after aortic valve replacement

Two standard prophylactic treatments of thrombosis within the first 3 months postsurgery currently used in our institution: a) daily dose of aspirin (325 mgs; b) daily dose of aspirin (81 mg) plus Warfarin for target INR 2.0-2.5

Sponsors

Ottawa Heart Institute Research Corporation
Lead SponsorOTHER
Edwards Lifesciences
CollaboratorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing primary aortic valve replacement with bioprosthetic (tissue) valve.

Exclusion criteria

* Emergency surgery or redo operations. * Patients with history of transient ischemic attacks, stroke, or history of carotid stenosis greater than 50% as detected by carotid duplex doppler or angiography. * Patients with COPD who are CO2 retainers. * Patients with LV function less than 50%, or enlarged left ventricle greater than 50 mm as detected by echocardiography or previous history of thromboembolism. * Patients with history of atrial fibrillation or heart rhythm disturbances.

Design outcomes

Primary

MeasureTime frameDescription
Differences in the Rate of Doppler-detected Cerebral Micro Emboli Between the Two Prophylactic Treatments of Thrombosis1 month after surgeryTrans-cranial doppler (TCD) measurements were used to test for the presence of cerebral micro-emboli. Doppler measurements were completed on the neck and throughout the temporal window. In addition, probes were secure to the temporal areas with a headband. Measurements determined presence of air or solid emboli. Each participant at the 1 month visit underwent TCD measurements after 30min of exposure to room air, and again 30min after receiving 100% oxygen through a breathing mask. Results show the comparison of participants on aspirin only vs warfarin + aspirin when TCD was completed both in room air and with 100% oxygen.

Secondary

MeasureTime frame
Differences in the Degree of Inhibition of Platelet Aggregation Between the Two Prophylactic Treatments of Thrombosis1 month after surgery
Difference in the Degree of Inhibitor of Platelet Aggregation Between the Two Prophylactic Treatments of Thrombosis1 month after surgery

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORMarc Ruel, MD, MPH

Ottawa Heart Institute Research Corporation

STUDY_DIRECTORThierry Mesana, MD, PhD

Ottawa Heart Institute Research Corporation

Participant flow

Recruitment details

Because all nonexcluded patients completed the study's procedures, the study was stopped after a total of 56 patients were enrolled and followed, with each arm of the study having 28 patients.

Baseline characteristics

Characteristic
Age, Continuous71.5 years
STANDARD_DEVIATION 9.5
Aortic cross clamp time81.5 minutes
STANDARD_DEVIATION 24
Cardiopulmonary Bypass time110 minutes
STANDARD_DEVIATION 42
Carotid artery stenosis <70%2 Participants
Coagulopathy0 Participants
Diabetes mellitus9 Participants
Heart Failure32 Participants
Hypertension21 Participants
Malignancy0 Participants
Post operative complications - Bleeding, >3 units PRBCs transfused3 Participants
Post operative complications - stroke/TIA0 Participants
Sex: Female, Male
Female
16 Participants
Sex: Female, Male
Male
19 Participants
Smoking4 Participants
Thrombocytosis/thrombocytopenia0 Participants
Type of surgery
bAVR + CABG
12 Participants
Type of surgery
bAVR only
16 Participants
Type of valve
Hancock II
8 Participants
Type of valve
Mosaic
1 Participants
Type of valve
Perimount
22 Participants
Vertebral artery stenosis1 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 280 / 28
other
Total, other adverse events
0 / 280 / 28
serious
Total, serious adverse events
0 / 280 / 28

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026