Anticoagulation Regimens in Pregnant Patients With Prosthetic Heart Valves

Sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02240927
Collaborator
(none)
40
1
4
71
0.6

Study Details

Study Description

Brief Summary

Pregnancy is associated with increased risk of thrombosis among women with mechanical prosthetic heart valves.However, the best anticoagulant treatment strategies for pregnant patients with prosthetic heart valves have been controversial. In this study the investigators wanted to identify the most effective and safe regimen among different anticoagulant regimens.

Condition or Disease Intervention/Treatment Phase
  • Drug: Low Molecular Weight Heparine : Enoxaparine
  • Drug: Enoxaparine and 2.5 mg Warfarin
  • Drug: Enoxaparine and 4mg Warfarin
  • Drug: Warfarin
N/A

Detailed Description

Four different anticoagulant treatment regimens for pregnant patients with prosthetic heart valves have been described. In the first arm warfarin is stopped and enoxaparine is started in 1mg/kg dose twice a day which is monitored by weekly anti-Xa levels (between 0.7-1.2) during the first trimester and followed by only warfarin after first trimester. In the second arm, if the patient's warfarin consumption is more than 5 mg before pregnancy, warfarin dose is decreased to 2.5 mg during the first trimester combined with enoxaparine in 1mg/kg dose twice a day; adjusted by measurements of anti-Xa levels (between 0.5-1) weekly until the end of 12th week of pregnancy . In the third arm warfarin dose is decreased to 4 mg during the first trimester combined with enoxaparine given in a similar manner. If the patient's therapeutic warfarin dose is less than 5 mg before pregnancy, warfarin is continued in the same dose during all the pregnancy in the 4th arm. All patients are followed by serial transesophageal echocardiography performed at 0,3,6 and 9. months of pregnancy. Informed consent is taken from all patients. After delivery the babies are examined by a experinced pediatrician and pediatric cardiologist for any congenital anomalies.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Different Anticoagulation Regimens in Pregnant Patients With Prosthetic Heart Valves: A Randomized Clinical Trial
Study Start Date :
Jan 1, 2010
Anticipated Primary Completion Date :
Jun 1, 2015
Anticipated Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Enoxaparine

During first trimester, warfarin is stopped and enoxaparine is started in 1mg/kg dose twice a day. Dose is adjusted according to Anti Factor Xa levels (between 0.7-1.2). Full dose warfarin is continued after first trimester and dose is regulated according to INR level (between 2.5-4).

Drug: Low Molecular Weight Heparine : Enoxaparine
During first trimester, warfarin is stopped and enoxaparine is started in 1mg/kg dose twice a day. Dose is adjusted according to Anti Factor Xa levels (between 0.7-1.2). Full dose warfarin is continued after first trimester and dose is regulated according to INR level (between 2.5-4).
Other Names:
  • Clexane
  • Active Comparator: Enoxaparine and 2.5 mg warfarin

    If the patient's therapeutic warfarin dose is more than 5 mg before pregnancy, warfarin dose is decreased to 2.5 mg during the first trimester and combined with enoxaparine in 1mg/kg dose twice a day. Enoxaparine dose is adjusted according to anti-factor Xa levels (between 0.5-1.0). Full dose warfarin is continued after first trimester and dose is regulated according to INR (between 2.5-4)

    Drug: Enoxaparine and 2.5 mg Warfarin
    If the patient's therapeutic warfarin dose is more than 5 mg before pregnancy, warfarin dose is decreased to 2.5 mg during the first trimester and combined with enoxaparine in 1mg/kg dose twice a day. Enoxaparine dose is adjusted according to anti-factor Xa levels (between 0.5-1). Full dose warfarin is continued after first trimester and dose is regulated according to INR level (between 2.5-4)
    Other Names:
  • Clexane and 2.5 mg Warfarin
  • Active Comparator: Enoxaparine and 4 mg warfarin

    If the patient's warfarin consumption dose is more than 5 mg before pregnancy, warfarin dose is decreased to 4 mg during the first trimester and combined with enoxaparine in 1mg/kg dose twice a day. Enoxaparine dose is adjusted according to anti-factor Xa levels (between 0.5-1). Full dose warfarin is continued after first trimester and dose is regulated according to INR level (between 2.5-4).

    Drug: Enoxaparine and 4mg Warfarin
    If the patient's warfarin consumption dose is more than 5 mg before pregnancy, warfarin dose is decreased to 4 mg during the first trimester and combined with enoxaparine in 1mg/kg dose twice a day. Enoxaparine dose is adjusted according to anti-factor Xa levels (between 0.5-1). Full dose warfarin is continued after first trimester and dose is regulated according to INR level (between 2.5-4).
    Other Names:
  • Clexane and 4 mg Warfarin
  • Active Comparator: Warfarin

    If the patient's therapeutic warfarin dose is less than 5 mg before pregnancy, warfarin is continued in the same dose during all the pregnancy and the dose is adjusted according to INR level (between 2.5-4).

    Drug: Warfarin
    If the patient's therapeutic warfarin dose is less than 5 mg before pregnancy, warfarin is continued in the same dose during all the pregnancy and the dose is adjusted according to INR level (between 2.5-4).

    Outcome Measures

    Primary Outcome Measures

    1. Successful pregnancy [12 month]

      In the absence of fetal and maternal fatal or nonfatal major complications successful pregnancy

    2. Maternal Complications [Participants will be followed during pregnancy and postpartum period, an expected average of 12 months]

      Nonfatal major complication: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion, abortus, placental hemorrhage, Assessment of an increase in thrombus burden more than 50% and/or progression of PVT obstruction by transesophageal echocardiography. Nonfatal minor complication: Bleeding without need for transfusion, TIA.

    3. Fetal Complications [12 months]

      Any congenital anomalia which may be attributed to warfarin or enoxaparine usage during pregnancy

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Pregnant patients with prosthetic heart valves
    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Kosuyolu Kartal Heart Training and Research Hospital Istanbul Turkey 34844

    Sponsors and Collaborators

    • Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital

    Investigators

    • Principal Investigator: Mehmet Ozkan, Prof, Kosuyolu Kartal Heart Training and Research Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    MEHMET OZKAN, Principal Investigator, MD., Prof., Head of Cardiology, Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
    ClinicalTrials.gov Identifier:
    NCT02240927
    Other Study ID Numbers:
    • KOSUYOLU1
    First Posted:
    Sep 16, 2014
    Last Update Posted:
    Sep 16, 2014
    Last Verified:
    Sep 1, 2014
    Keywords provided by MEHMET OZKAN, Principal Investigator, MD., Prof., Head of Cardiology, Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 16, 2014