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Not yet recruitingNCT05687448DIAMONDUpdated Jun 12, 2025

DIrect Oral Anticoagulation and Bioprothesis Aortic Valve

A Phase 3 interventional study of Apixaban 5 MG Oral Tablet and Aspirin 75 to 100mg once a day in Aortic Valve Disease, sponsored by Assistance Publique - Hôpitaux de Paris. Not yet recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-06-12.

Sponsored by Assistance Publique - Hôpitaux de Paris · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Phase 3
Study type
Interventional
Enrollment
1,500
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

DIAMOND study is a national, multicentre, randomized, parallel-group, open label study in patients (aged ≥18 years) with aortic bioprosthesis (excluding TAVI) at least 7 days after cardiac surgery.

Experimental group:

Patients treated with apixaban 5 mg twice daily (BID)

Active Comparator group:

Aspirin 75 to 100mg once a day

The primary objective is to demonstrate that antithrombotic treatment with apixaban is superior to aspirin in patients with recent surgical bioprosthetic aortic valve replacement for the primary composite efficacy endpoint of death from any cause, myocardial infarction, stroke, systemic embolism, deep vein thrombosis, or pulmonary embolism and valve thrombosis after 105 days of follow-up.

Read the detailed description

Early antithrombotic management of patients who have undergone aortic valve replacement using a bioprosthesis remains a source of medical concern. The optimal antithrombotic strategy early after surgery remains controversial due to lack of high-quality evidence. Some observational studies support the use of vitamin K antagonists (VKAs) compared to aspirin (ASA) to significantly reduce the risk of thromboembolism but suffer from major source of bias inherent to retrospective analyses of observational data. A small, randomized trial found that VKA for 3 months significantly increased major bleeding compared with ASA, without reducing the rate of deaths or thromboembolic events but this study was underpowered for ischemic events. There is therefore a lack of evidence demonstrating the superiority of anticoagulant treatment compared to aspirin early after bioprosthetic aortic valve surgery. Current ESC guidelines recommend that ASA or VKA should be considered for 3 months after surgical implantation of an aortic bioprosthesis. At the opposite, current AHA/ACC guidelines recommend that anticoagulation with VKA to achieve an INR of 2.5 is reasonable for at least 3 months and for as long as 6 months for patients at low risk of bleeding (IIa, level B). However, anticoagulation by VKAs is currently underused and guideline recommendations are not followed by most clinicians as VKAs have major drawbacks: narrow therapeutic window, variable dose-response in individuals, interaction with several foods and drugs.

Despite their superiority to reduce bleeding in patients with non-valvular atrial fibrillation compared to VKAs, direct oral anticoagulants (DOACs) including apixaban have not been well evaluated in the first 3 months after surgical bioprosthetic valve implantation. A small, randomized trial found that edoxaban was non-inferior to warfarin for preventing thromboembolism and the occurrence of major bleeding in the first 3 months after aortic or mitral surgical bioprosthetic valve implantation. DOAC(s) are effective in patients with atrial fibrillation and bioprosthetic valve implanted after 3 months.

Finally, there is an unmet clinical need for an alternative to ASA or VKAs, such as an anti-Xa DOAC like apixaban, as anticoagulation in patients in the first 3 months after surgical bioprosthetic valve implantation.

The purpose of this study is to compare the efficacy of apixaban and aspirin on ischemic endpoints during the first 3 months after aortic surgical bioprosthetic valve implantation excluding TAVI.

02

Conditions studied

  • Aortic Valve Disease

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Keywords

  • Anticoagulant
  • Aortic valve
  • Apixaban
  • Aspirin
  • Stroke
  • Hemorrhage
03

In context

Aortic Valve Disease

231 studies on the registry are indexed under Aortic Valve Disease; 76 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 108 across 116 interventional studies indexed under Aortic Valve Disease.

Browse Aortic Valve Disease studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 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

Inclusion criteria

  1. Male or female ≥18 years of age
  2. Prior implantation of a surgical bioprosthesis in the aortic position at least 7 days and before hospital discharge (excluding TAVI)
  3. Participants currently not requiring chronic anticoagulation for another reason (atrial fibrillation, pulmonary embolism or any other condition)
  4. Patients affiliated to social security
  5. Patient able to give free, informed and written consent

Exclusion criteria

Exclusion Criteria:

  1. Any cardiac surgery less than 7 days prior to enrollment or more than 1 month
  2. Mechanical valve in any position or combined valve surgery (mitral or tricuspid).
  3. Any major bleeding in the three months (90 days) prior to enrollment.
  4. Active bleeding or high risk of bleeding after cardiac surgery (i.e. hemopericardium) or lesion or condition considered as a significant risk factor for major bleeding according to investigator
  5. Atrial fibrillation requiring chronic anticoagulation
  6. Need to be on dual antiplatelet therapy (aspirin >100 mg daily and a P2Y12 inhibitor, i.e. clopidogrel, ticagrelor, prasugrel) or requiring chronic anticoagulation whatever the treatment (oral or injection).
  7. Known hypersensitivity or other contraindications to apixaban (hepatic disease associated with coagulopathy and clinically relevant bleeding risk).
  8. Creatinine clearance \<40 mL/min (Cockcroft) or patients requiring apixaban dose reduction.
  9. Known hypersensitivity or other contraindications to aspirin (Hypersensitivity to aspirin or any of the excipients, history of asthma induced by the administration of salicylates, ongoing peptic ulcer, constitutional or acquired hemorrhagic disease including gastrointestinal bleeding, history of hemorrhagic stroke and thrombocytopenia, pregnancy after 24 weeks of gestation, risk of bleeding, severe renal failure, severe hepatic impairment, uncontrolled severe heart failure
  10. Known hypersensitivity or other contraindications to heparin or low molecular weight heparin (history of heparin-induced thrombocytopenia, hypersensitivity to any of the excipients...)
  11. Ischemic stroke within 1 month or intracranial hemorrhage
  12. Active endocarditis at the time of screening for enrollment.
  13. Women of childbearing potential without efficient contraception, pregnant or breastfeeding women.
  14. Concomitant combined strong P-gp and CYP3A4 inducers or inhibitors.
  15. History of non-compliance
  16. Participation in another interventional study
  17. Active cancer or life expectancy less than 1 year
  18. Persons deprived of their liberty by judicial or administrative decision
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,500 participants (estimated)

Study arms

  • Experimental
    Experimental Group

    Patients treated with apixaban 5 mg twice daily (BID)

    Drug: Apixaban 5 MG Oral Tablet

  • Active comparator
    Active Comparator group:

    Patients treated with Aspirin 75 to 100mg once a day

    Drug: Aspirin 75 to 100mg once a day

Interventions

  • DrugApixaban 5 MG Oral Tablet

    Patients treated with apixaban 5 mg twice daily (BID)

    Also known as: Experimental Group

  • DrugAspirin 75 to 100mg once a day

    Patients treated with Aspirin 75 to 100mg once a day

    Also known as: Active Comparator

06

What researchers measure

Primary outcomes

  1. Major Adverse Clinical Events (MACE)

    The primary endpoint is a composite efficacy endpoint including death from any cause, myocardial infarction, stroke, systemic embolism, deep vein thrombosis, or pulmonary embolism and valve thrombosis.

    Time frame: Up to 3.5 months

Secondary outcomes

  1. Bleeding

    ISTH major and non-major clinically relevant bleeding

    Time frame: Up to 3.5 months

  2. Death

    Including cardiovascular and non cardiovascular death

    Time frame: Up to 3.5 months

  3. Myocardial infarction

    Time frame: Up to 3.5 months

  4. Stroke

    Time frame: Up to 3.5 months

  5. Systemic embolism

    Time frame: Up to 3.5 months

  6. Deep vein thrombosis or pulmonary embolism

    Time frame: Up to 3.5 months

  7. Valve thrombosis

    Time frame: Up to 3.5 months

  8. Bleeding

    According to ISTH major and non-major clinically relevant bleeding, BARC and TIMI 6, BARC and TIMI Classifications

    Time frame: Up to 3.5 months

  9. Echographic parameter of aortic valve

    Variation of mean aortic gradient (mm/Hg)

    Time frame: Up to 3.5 months

  10. Assessment of coagulation

    Measured by thrombin generation in a subgroup population (n=216)

    Time frame: Up to 3.5 months

  11. To evaluate platelet activation (sP-selectin) in a subgroup population (n = 216)

    Time frame: Up to 3.5 months

  12. To build a population PK/PD in the experimental group

    Measuring the apixaban concentration (anti-Xa activity expressed in ng/mL) (apixaban, n = 108)

    Time frame: Up to 3.5 months

07

Study locations

1 site
  • Service de Cardiologie Hôpital Lariboisière
    Paris, 75010, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05687448
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Responsible party
Sponsor
First posted
Jan 18, 2023
Start date
Sep 2025 (estimated)
Primary completion
Sep 2025 (estimated)
Completion
Mar 2029 (estimated)
Last update
Jun 12, 2025

Study contacts

Jean-Guillaume DILLINGER, Professor
Contact
jean-guillaume.dillinger@aphp.fr
+33 1 49 95 86 74
Bernard IUNG, Professor
Contact
bernard.iung@aphp.fr
+33 1 40 25 66 01
Jean-Guillaume DILLINGER, Professor
principal investigator · Assistance Publique Hôpitaux Paris

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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