TROIA: Comparison of Different TRansesophageal Echocardiography Guided thrOmbolytic Regimens for prosthetIc vAlve Thrombosis

Sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01451320
Collaborator
(none)
182
1
5
203
0.9

Study Details

Study Description

Brief Summary

Despite high mortality and morbidity, the best treatment strategies for prosthetic valve thrombosis (PVT) have been controversial. In this study the investigators wanted to identify the most effective and safe regimen among different thrombolytic strategies.Transesophageal echocardiography (TEE) guided thrombolytic treatment was administered to 182 consecutive patients with PVT in 220 different episodes (156 women, mean age 43.2±13.06 years) between 1993 and 2009. These regimens included rapid streptokinase (Group I, 16 episodes), slow streptokinase (Group II, 41 episodes), high dose (100 mg) tissue plasminogen activator (t-PA) (Group III, 12 episodes), half-dose (50 mg) slow infusion (6-hours) of t-PA without bolus (Group IV, 27 episodes), and low dose (25 mg) and slow infusion (6-hours) of t-PA without bolus (Group V, 124 episodes). The study endpoints were thrombolytic success and in-hospital mortality and non-fatal complication rates.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

One hundred and eighty two consecutive in-hospital patients with 220 episodes of PVT between 1993 and 2009 were included in the study. The patients were enrolled after informed consent if there was no contraindication, to thrombolysis. The study was approved by the local Ethics Board. The patient demographics, past medical history, date of the operation, type and make of the prosthetic valve, rhythm disorders, aspirin use, NYHA functional capacity, leading symptoms and international normalization ratio (INR) values at the time of admission were prospectively entered into a database.The diagnosis of PVT was verified each time by transesophageal echocardiography (TEE) when a patient was admitted with thromboembolism or persistently low INR for the preceding consecutive 3 months and when a transthoracic echocardiography (TTE) documented prosthetic valve dysfunction or thrombus. All patients underwent TTE and TEE examination before and after the thrombolysis sessions. The cross sectional area and the longest diameter of the thrombus were measured on TEE recordings

Study Design

Study Type:
Interventional
Actual Enrollment :
182 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Different TRansesophageal Echocardiography Guided thrOmbolytic Regimens for prosthetIc vAlve Thrombosis
Study Start Date :
Jan 1, 1993
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: rapid streptokinase

3-hour infusion of 1.5 million units of streptokinase (16 patients, 16 episodes), repeat once 24 hours later if needed (maximum total dose 3 million units).

Drug: Streptokinase
3-hour infusion of 1.5 million units of streptokinase (16 patients, 16 episodes), repeat once 24 hours later if needed (maximum total dose 3 million units)
Other Names:
  • Streptase
  • Active Comparator: high dose tpa

    5-hour infusion of 90 mg t-PA(Tissue plasminogen activator) after 10 mg bolus (10 patients, 12 episodes), repeat once 24 hours later if needed (maximum total dose 200 mg)

    Drug: Tissue plasminogen activator
    5-hour infusion of 90 mg t-PA (Tissue plasminogen activator) after 10 mg bolus (10 patients, 12 episodes), repeat once 24 hours later if needed (maximum total dose 200 mg)
    Other Names:
  • ACTILYSE
  • Active Comparator: slow streptokinase

    24-hour infusion of 1.5 million units of streptokinase (41 patients, 41 episodes), repeat once 24 hours later if needed (maximum total dose 3 million units).

    Drug: Streptokinase
    24-hour infusion of 1.5 million units of streptokinase (41 patients, 41 episodes), repeat once 24 hours later if needed (maximum total dose 3 million units).
    Other Names:
  • Streptase
  • Active Comparator: half-dose slow infusion tpa

    6-hour infusion of 50 mg t-PA (Tissue plasminogen activator) without bolus (27 patients, 27 episodes), repeat once 24 hours later up to 3 times if needed (maximum total dose 150 mg).

    Drug: Tissue Plasminogen Activator
    6-hour infusion of 50 mg t-PA (Tissue plasminogen activator) without bolus (27 patients, 27 episodes), repeat once 24 hours later up to 3 times if needed (maximum total dose 150 mg).
    Other Names:
  • ACTILYSE
  • Active Comparator: low dose slow infusion tpa

    6-hour infusion of 25 mg t-PA(Tissue plasminogen activator) without bolus (108 patients, 124 episodes), repeat once 24 hours later up to 6 times if needed (maximum total dose 150 mg).

    Drug: Tissue Plasminogen Activator
    6-hour infusion of 25 mg t-PA (Tissue plasminogen activator) without bolus (108 patients, 124 episodes), repeat once 24 hours later up to 6 times if needed (maximum total dose 150 mg).
    Other Names:
  • ACTILYSE
  • Outcome Measures

    Primary Outcome Measures

    1. Thrombolytic success [24 hours]

      In the absence of fatal or nonfatal major complications; Obstructive thrombus: Doppler documentation of the resolution of increased gradient and decreased valve area. Clinical improvement in symptoms. Reduction by ≥75% in major diameter or area of the thrombus. Complete success was defined when all 3 criteria were met and partial success was defined as less than 3. Nonobstrucive thrombus: Complete success: ≥75% reduction in thrombus area. Partial success: 50%-75% reduction in thrombus area.

    2. Non-fatal complication rates [participants will be followed for the duration of hospital stay, an expected average of 3 weeks]

      Nonfatal major complication: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion. Nonfatal minor complication: Bleeding without need for transfusion, TIA.

    3. In-hospital mortality [participants will be followed for the duration of hospital stay, an expected average of 3 weeks]

      All cause in-hospital mortality.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with prosthetic valve thrombosis
    Exclusion Criteria:
    • Large left atrial thrombus

    • Recent (<3 weeks) ischemic stroke

    • Hemorrhagic stroke

    • Early (<4 days) postoperative period

    • Traumatic accident <4 weeks

    • Bleeding diathesis †

    • İntracranial mass

    • Active internal bleed

    • Aortic dissection

    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, Assoc.Prof., Kosuyolu Kartal Heart Training and Research Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    MEHMET OZKAN, Principal Investigator, MD., FESC., Assoc. Prof,. Head of Cardiology, Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
    ClinicalTrials.gov Identifier:
    NCT01451320
    Other Study ID Numbers:
    • 11
    First Posted:
    Oct 13, 2011
    Last Update Posted:
    Oct 13, 2011
    Last Verified:
    Oct 1, 2011
    Keywords provided by MEHMET OZKAN, Principal Investigator, MD., FESC., Assoc. Prof,. Head of Cardiology, Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 13, 2011