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Thrombolytic Therapy Versus Surgery for Obstructive Prosthetic Valve Thrombosis

Primary Purpose

Obstructive Thrombus

Status
Unknown status
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Thrombolytic Therapy
Surgery
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 Obstructive Thrombus focused on measuring Prosthetic valve, Thrombosis, Surgery, Thrombolytic therapy, Transesophageal echocardiography

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obstructive prosthetic valve thrombosis

Exclusion Criteria:

  • Non-obstructive prosthetic valve thrombosis

Sites / Locations

  • Kosuyolu Kartal Heart Training and Research HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Thrombolytic therapy

Surgery

Arm Description

In the first arm, thrombolytic therapy (TT) is performed to the patients with obstructive prosthetic valve thrombosis. The TT regimen depends on the functional status of the patient. In patients with NYHA class III-IV dyspnea low dose, relatively faster TT regimen (25 mg tPA/6 hours) is performed. In patients with NYHA class I-II dyspnea TT with low dose and ultra-slow infusion of tPA (25 mg tPA/25 hours) is performed. During TT, patients are followed up with transesophageal echocardiography in every 24 hours.

In the second arm, redo valve surgery is performed for obstructive valve thrombosis. Intraoperative and postoperative results are recorded

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 complications for thrombolytic therapy
Nonfatal major complication: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion. Nonfatal minor complication: Bleeding without need for transfusion, TIA.
Successful Surgery
Successful redo valve surgery in the absence of fatal and non fatal major complications.
Complications for surgery
Non fatal major complications: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion, pericardial tamponade, sepsis, pacemaker requirement, mediastinitis, wound infections, acute renal failure Minor complications: bleeding requiring transfusion, plevral effusion, pericardial effusion without tamponade
In hospital mortality
All cause in-hospital mortality.

Secondary Outcome Measures

Full Information

First Posted
September 12, 2014
Last Updated
September 16, 2014
Sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02243839
Brief Title
Thrombolytic Therapy Versus Surgery for Obstructive Prosthetic Valve Thrombosis
Official Title
Thrombolytic Therapy Versus Surgery for Obstructive Prosthetic Valve Thrombosis: A Randomized Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

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
Prosthetic heart valve thrombosis is a serious complication with high mortality and morbidity The best treatment of PVT is controversial, although surgery and thrombolysis options have been available. In this randomized and multicenter study, the investigators compared thrombolytic therapy versus surgery for the treatment of patients with obstructive prosthetic valve thrombosis.
Detailed Description
Two different randomization group have been defined and patients with obstructive prosthetic valve thrombosis are included in each group randomly. In the first arm, thrombolytic therapy (TT) is performed to the patients with obstructive prosthetic valve thrombosis. The TT regimen depends on the functional status of the patient. In patients with NYHA class III-IV dyspnea low dose, relatively faster TT regimen (25 mg tPA/6 hours) is performed. In patients with NYHA class I-II dyspnea TT with low dose and ultra slow infusion of tPA (25 mg tPA/25 hours) is performed. During TT, patients are followed up with transesophageal echocardiography in every 24 hours. In the second arm, redo valve surgery is performed for obstructive valve thrombosis. This multicenter study is conducted in Cardiology and Cardiovascular Surgery Departments of Kosuyolu Kartal Heart Training and Research Hospital, Istanbul, Turkey, Siyami Ersek Heart Training and Research Hospital, Istanbul, Turkey, Ankara Heart Training and Research Hospital, Ankara, Turkey, İzmir Atatürk Heart Training and Research Hospital, İzmir, Turkey, Erzurum Atatürk University Faculty of Medicine, Erzurum, Turkey, Diyarbakır Dicle University Faculty of Medicine, Diyarbakır, Turkey and Kars Kafkas University Faculty of Medicine, Kars, Turkey. Informed consent is taken from all patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Thrombus
Keywords
Prosthetic valve, Thrombosis, Surgery, Thrombolytic therapy, Transesophageal echocardiography

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Thrombolytic therapy
Arm Type
Active Comparator
Arm Description
In the first arm, thrombolytic therapy (TT) is performed to the patients with obstructive prosthetic valve thrombosis. The TT regimen depends on the functional status of the patient. In patients with NYHA class III-IV dyspnea low dose, relatively faster TT regimen (25 mg tPA/6 hours) is performed. In patients with NYHA class I-II dyspnea TT with low dose and ultra-slow infusion of tPA (25 mg tPA/25 hours) is performed. During TT, patients are followed up with transesophageal echocardiography in every 24 hours.
Arm Title
Surgery
Arm Type
Active Comparator
Arm Description
In the second arm, redo valve surgery is performed for obstructive valve thrombosis. Intraoperative and postoperative results are recorded
Intervention Type
Drug
Intervention Name(s)
Thrombolytic Therapy
Intervention Description
Thrombolytic therapy is performed to the patients with obstructive prosthetic valve thrombosis
Intervention Type
Procedure
Intervention Name(s)
Surgery
Intervention Description
Redo valve surgery is performed for obstructive valve thrombosis
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
Up to 10 days
Title
Non-fatal complications for thrombolytic therapy
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
Successful Surgery
Description
Successful redo valve surgery in the absence of fatal and non fatal major complications.
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 3 weeks; and postoperative 3 months
Title
Complications for surgery
Description
Non fatal major complications: Ischemic stroke, intracranial hemorrhage, embolism (coronary or peripheral), bleeding requiring transfusion, pericardial tamponade, sepsis, pacemaker requirement, mediastinitis, wound infections, acute renal failure Minor complications: bleeding requiring transfusion, plevral effusion, pericardial effusion without tamponade
Time Frame
Participants will be followed for the duration of hospital stay an expected average of 3 weeks; and postoperative 3 month
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
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Obstructive prosthetic valve thrombosis Exclusion Criteria: Non-obstructive prosthetic valve thrombosis
Facility Information:
Facility Name
Kosuyolu Kartal Heart Training and Research Hospital
City
İstanbul
ZIP/Postal Code
34844
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mehmet Özkan, Prof
Phone
905322551512
Email
memoozkan1@gmail.com
First Name & Middle Initial & Last Name & Degree
Mehmet Özkan, Professor

12. IPD Sharing Statement

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Thrombolytic Therapy Versus Surgery for Obstructive Prosthetic Valve Thrombosis

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