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

Primary Purpose

Prosthetic Valve Thrombosis

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Streptokinase
Streptokinase
Tissue plasminogen activator
Tissue Plasminogen Activator
Tissue Plasminogen Activator
Sponsored by
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prosthetic Valve Thrombosis focused on measuring Prosthetic valve, thrombosis, TROIA, tPA, TEE

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Kosuyolu Kartal Heart Training and Research Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

rapid streptokinase

high dose tpa

slow streptokinase

half-dose slow infusion tpa

low dose slow infusion tpa

Arm Description

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).

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)

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).

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).

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).

Outcomes

Primary Outcome Measures

Thrombolytic success
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.
Non-fatal complication rates
Nonfatal major complication: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion. Nonfatal minor complication: Bleeding without need for transfusion, TIA.
In-hospital mortality
All cause in-hospital mortality.

Secondary Outcome Measures

Full Information

First Posted
September 29, 2011
Last Updated
October 11, 2011
Sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01451320
Brief Title
Comparison of Different TRansesophageal Echocardiography Guided thrOmbolytic Regimens for prosthetIc vAlve Thrombosis
Acronym
TROIA
Official Title
Comparison of Different TRansesophageal Echocardiography Guided thrOmbolytic Regimens for prosthetIc vAlve Thrombosis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2011
Overall Recruitment Status
Completed
Study Start Date
January 1993 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital

4. Oversight

Data Monitoring Committee
No

5. 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.
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prosthetic Valve Thrombosis
Keywords
Prosthetic valve, thrombosis, TROIA, tPA, TEE

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
182 (Actual)

8. Arms, Groups, and Interventions

Arm Title
rapid streptokinase
Arm Type
Active Comparator
Arm Description
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).
Arm Title
high dose tpa
Arm Type
Active Comparator
Arm Description
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)
Arm Title
slow streptokinase
Arm Type
Active Comparator
Arm Description
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).
Arm Title
half-dose slow infusion tpa
Arm Type
Active Comparator
Arm Description
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).
Arm Title
low dose slow infusion tpa
Arm Type
Active Comparator
Arm Description
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).
Intervention Type
Drug
Intervention Name(s)
Streptokinase
Other Intervention Name(s)
Streptase
Intervention Description
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)
Intervention Type
Drug
Intervention Name(s)
Streptokinase
Other Intervention Name(s)
Streptase
Intervention Description
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).
Intervention Type
Drug
Intervention Name(s)
Tissue plasminogen activator
Other Intervention Name(s)
ACTILYSE
Intervention Description
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)
Intervention Type
Drug
Intervention Name(s)
Tissue Plasminogen Activator
Other Intervention Name(s)
ACTILYSE
Intervention Description
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).
Intervention Type
Drug
Intervention Name(s)
Tissue Plasminogen Activator
Other Intervention Name(s)
ACTILYSE
Intervention Description
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).
Primary Outcome Measure Information:
Title
Thrombolytic success
Description
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.
Time Frame
24 hours
Title
Non-fatal complication rates
Description
Nonfatal major complication: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion. Nonfatal minor complication: Bleeding without need for transfusion, TIA.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 3 weeks
Title
In-hospital mortality
Description
All cause in-hospital mortality.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 3 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mehmet Ozkan, Assoc.Prof.
Organizational Affiliation
Kosuyolu Kartal Heart Training and Research Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kosuyolu Kartal Heart Training and Research Hospital
City
Istanbul
ZIP/Postal Code
34844
Country
Turkey

12. IPD Sharing Statement

Citations:
PubMed Identifier
10841239
Citation
Ozkan M, Kaymaz C, Kirma C, Sonmez K, Ozdemir N, Balkanay M, Yakut C, Deligonul U. Intravenous thrombolytic treatment of mechanical prosthetic valve thrombosis: a study using serial transesophageal echocardiography. J Am Coll Cardiol. 2000 Jun;35(7):1881-9. doi: 10.1016/s0735-1097(00)00654-9.
Results Reference
background
PubMed Identifier
23489534
Citation
Ozkan M, Gunduz S, Biteker M, Astarcioglu MA, Cevik C, Kaynak E, Yildiz M, Oguz E, Aykan AC, Erturk E, Karavelioglu Y, Gokdeniz T, Kaya H, Gursoy OM, Cakal B, Karakoyun S, Duran N, Ozdemir N. Comparison of different TEE-guided thrombolytic regimens for prosthetic valve thrombosis: the TROIA trial. JACC Cardiovasc Imaging. 2013 Feb;6(2):206-16. doi: 10.1016/j.jcmg.2012.10.016.
Results Reference
derived

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

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