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Recombinant Streptokinase Versus Urokinase in Pulmonary Embolism in China (RESUPEC) (RESUPEC)

Primary Purpose

Pulmonary Embolism, Pulmonary Thromboembolism

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Recombinant Streptokinase
Urokinase
Sponsored by
Beijing Chao Yang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Embolism focused on measuring pulmonary embolism, thrombolysis, massive, submassive, recombinant streptokinase, urokinase

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Symptomatic PTE confirmed either by CTPA or by a high probability ventilation-perfusion lung scanning (V/Q scan).
  • Presented with hemodynamic instability (systolic blood pressure <90 mmHg or a fall in systolic blood pressure of more than 40 mmHg for at least 15 min, or cardiogenic shock) or associated with RVD identified by echocardiography or CT.
  • Symptoms deterioration less than 14 days before diagnosis.

Exclusion Criteria:

  • Active bleeding or spontaneous intracranial hemorrhage in the preceding 6 months
  • Major surgery, organ biopsy or recent puncture of a non-compressible vessel in the preceding 2 weeks
  • Cerebral arterial thrombosis in the preceding 2 months
  • Gastro-intestinal bleeding in the preceding 10 days
  • Major trauma within the past 15 days
  • Neurosurgery or ophthalmologic operation in the preceding 1 month
  • Uncontrolled hypertension (systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 110 mmHg)
  • Recent external cardiac resuscitation manoeuvres
  • Platelet count < 100,000/mm3 at admission
  • Pregnancy, puerperium or lactation in the preceding 2 weeks
  • Infectious pericarditis or endocarditis
  • Severe hepatic and kidney dysfunction
  • Hemorrhagic retinopathy due to diabetes
  • A known bleeding disorder.
  • Chronic thromboembolic pulmonary hypertension (CTEPH) without new pulmonary thromboembolism (PTE)
  • Received streptokinase in the preceding 6 months
  • Infected by streptococcus in the preceding 1 month.

Sites / Locations

  • Beijing Institute of Respiratory Medicine, Beijing Chao-Yang hospital
  • Guangdong Institute of Respiratory Disease, Guangzhou Medical University,
  • Shenzhen People's Hospital
  • The General Hospital of Shenyang Military Command
  • Affiliated Hospital of Ningxia Medical University
  • The Affiliated Hospital of Medical College Qingdao University
  • The First Affiliated Hospital of Shanxi Medical University
  • Tianjin Medical University General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

r-SK group

UK group

Arm Description

Recombinant streptokinase: 1.5 million IU continuously intravenous infusion for 2 hours

Urokinase: 20,000 IU/kg continuously intravenous infusion for 2 hours

Outcomes

Primary Outcome Measures

The improvement of the right ventricular function on echocardiogram
Quantitative computed tomographic pulmonary angiography (CTPA) score
The relief of symptoms

Secondary Outcome Measures

Major or minor bleeding
Pulmonary embolism recurrence
Death

Full Information

First Posted
August 28, 2009
Last Updated
August 31, 2009
Sponsor
Beijing Chao Yang Hospital
Collaborators
Qingdao University, Tianjin Medical University General Hospital, General Hospital of Shenyang Military Region, Guangdong Institute of Respiratory Disease, The First Affiliated Hospital of Shanxi Medical University, Shenzhen People's Hospital, Ningxia Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT00968929
Brief Title
Recombinant Streptokinase Versus Urokinase in Pulmonary Embolism in China (RESUPEC)
Acronym
RESUPEC
Official Title
Efficacy and Safety Evaluation of Recombinant Streptokinase and Urokinase in the Treatment of Pulmonary Embolism: A Multi-Center, Randomized Controlled Trial in China
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Beijing Chao Yang Hospital
Collaborators
Qingdao University, Tianjin Medical University General Hospital, General Hospital of Shenyang Military Region, Guangdong Institute of Respiratory Disease, The First Affiliated Hospital of Shanxi Medical University, Shenzhen People's Hospital, Ningxia Medical University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Recombinant streptokinase (r-SK) is an effective thrombolytic agent developed with gene engineering. Its characteristics of high output and low production cost make it affordable in treating acute myocardial infarction (AMI) in developing countries. It is unclear whether r-SK can be used in patients with pulmonary embolism (PE). The aim of this study was to investigate the efficacy and safety of 1.5 million IU r-SK by 2 hours infusion and 20,000 IU/kg urokinase (UK) by 2 hours infusion in selected PE patients.
Detailed Description
Pulmonary embolism (PE) is a common cardiovascular illness. Massive PE is characterized with cardiogenic shock and/or persistent arterial hypotension. Submassive PE patients are defined with right ventricular dysfunction (RVD) identified by echocardiography or CT and the etc. The mortality of massive and submassive PE is higher than low-risk PE. PE has the mortality rate of >15% in the first 3 months after diagnosis. Thrombolytic treatment should be commenced as soon as possible after high-risk PE was diagnosed. Thrombolysis has been proved to be the most rapid and effective therapy to reduce the obstruction of pulmonary circulation and normalize hemodynamic parameters. The ultimate goals of thrombolytic therapy for this disease are to minimize early morbidity and mortality and to prevent recurrence without provoking excessive bleeding. Currently, the choice of thrombolytic agents and regimens (SK, UK or rt-PA) is mostly based on personal or regional preferences. A novel dosing regimen of UK (3 million IU/2h, or 4400 IU/kg as a loading dose followed by 4400 IU/kg/h over 12h) and SK (1.5 million IU /2h) have been recommended in ESC guidelines. Considering lower body weight in Chinese population, a relative lower dosage UK-2h (20,000 IU/kg) regimen combined with low molecular weight heparin (LMWH) has been used in Chinese population. Our previous study has revealed that the efficacy and safety of UK-2h (20 000 IU/Kg) were similar with UK-12h (standard regimen) in Chinese patients. Thus the UK-2h (20,000 IU/Kg) became a popular and alternative choice in treating PE in China for its lower cost and convenience. Natural streptokinase (n-SK or SK) is an old thrombolytic agent. However, its immunogenicity lowers its safety and that constitute a concern among doctors. In recent years, as the development of gene engineering, r-SK was produced. R-SK has the advantage of not containing streptolysin and streptodornase unlike streptococci-derived n-SK which might make it safer theoretically. For its low cost, r-SK has been used to treat AMI especially in developing countries. In this study, the efficacy and safety between r-SK (1.5 million IU/2h) and UK-2h (20 000U/Kg) for treating acute PE will be compared. The study is conducted in patients with massive PE and submassive PE. The clinical efficacy, emboli dissolving efficacy and safety will be evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Embolism, Pulmonary Thromboembolism
Keywords
pulmonary embolism, thrombolysis, massive, submassive, recombinant streptokinase, urokinase

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
83 (Actual)

8. Arms, Groups, and Interventions

Arm Title
r-SK group
Arm Type
Experimental
Arm Description
Recombinant streptokinase: 1.5 million IU continuously intravenous infusion for 2 hours
Arm Title
UK group
Arm Type
Active Comparator
Arm Description
Urokinase: 20,000 IU/kg continuously intravenous infusion for 2 hours
Intervention Type
Drug
Intervention Name(s)
Recombinant Streptokinase
Intervention Description
Recombinant streptokinase: 1.5 million IU continuously intravenous infusion for 2 hours
Intervention Type
Drug
Intervention Name(s)
Urokinase
Intervention Description
Urokinase: 20,000 IU/kg continuously intravenous infusion for 2 hours
Primary Outcome Measure Information:
Title
The improvement of the right ventricular function on echocardiogram
Time Frame
within the 1st, 14 days and 3 months
Title
Quantitative computed tomographic pulmonary angiography (CTPA) score
Time Frame
1st, 14 days and 3 months
Title
The relief of symptoms
Time Frame
2-4h, 1st, 4th , 7th, 10th, 14 days day and 3 months
Secondary Outcome Measure Information:
Title
Major or minor bleeding
Time Frame
14 days and 3 months
Title
Pulmonary embolism recurrence
Time Frame
14 days and 3 months
Title
Death
Time Frame
14 days and 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic PTE confirmed either by CTPA or by a high probability ventilation-perfusion lung scanning (V/Q scan). Presented with hemodynamic instability (systolic blood pressure <90 mmHg or a fall in systolic blood pressure of more than 40 mmHg for at least 15 min, or cardiogenic shock) or associated with RVD identified by echocardiography or CT. Symptoms deterioration less than 14 days before diagnosis. Exclusion Criteria: Active bleeding or spontaneous intracranial hemorrhage in the preceding 6 months Major surgery, organ biopsy or recent puncture of a non-compressible vessel in the preceding 2 weeks Cerebral arterial thrombosis in the preceding 2 months Gastro-intestinal bleeding in the preceding 10 days Major trauma within the past 15 days Neurosurgery or ophthalmologic operation in the preceding 1 month Uncontrolled hypertension (systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 110 mmHg) Recent external cardiac resuscitation manoeuvres Platelet count < 100,000/mm3 at admission Pregnancy, puerperium or lactation in the preceding 2 weeks Infectious pericarditis or endocarditis Severe hepatic and kidney dysfunction Hemorrhagic retinopathy due to diabetes A known bleeding disorder. Chronic thromboembolic pulmonary hypertension (CTEPH) without new pulmonary thromboembolism (PTE) Received streptokinase in the preceding 6 months Infected by streptococcus in the preceding 1 month.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chen WANG, Prof
Organizational Affiliation
Beijing Institute of Respiratory Medicine, Beijing-Chao Yang Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Institute of Respiratory Medicine, Beijing Chao-Yang hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100020
Country
China
Facility Name
Guangdong Institute of Respiratory Disease, Guangzhou Medical University,
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Facility Name
Shenzhen People's Hospital
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518020
Country
China
Facility Name
The General Hospital of Shenyang Military Command
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110016
Country
China
Facility Name
Affiliated Hospital of Ningxia Medical University
City
Yinchuan
State/Province
Ningxia
ZIP/Postal Code
750004
Country
China
Facility Name
The Affiliated Hospital of Medical College Qingdao University
City
Qingdao
State/Province
Shandong
ZIP/Postal Code
266003
Country
China
Facility Name
The First Affiliated Hospital of Shanxi Medical University
City
Taiyuan
State/Province
Shanxi
ZIP/Postal Code
030001
Country
China
Facility Name
Tianjin Medical University General Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300052
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
17716753
Citation
Zhu L, Yang Y, Wu Y, Zhai Z, Wang C. Value of right ventricular dysfunction for prognosis in pulmonary embolism. Int J Cardiol. 2008 Jun 23;127(1):40-5. doi: 10.1016/j.ijcard.2007.06.093. Epub 2007 Aug 22.
Results Reference
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PubMed Identifier
17254482
Citation
Zhu L, Yang YH, Wu YF, Zhai ZG, Wang C; National Project of the Diagnosis and Treatment Strategies for Pulmonary Thromboembolism investigators. Value of transthoracic echocardiography combined with cardiac troponin I in risk stratification in acute pulmonary thromboembolism. Chin Med J (Engl). 2007 Jan 5;120(1):17-21.
Results Reference
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PubMed Identifier
17705052
Citation
Zhu L, Wang C, Yang Y, Wu Y, Zhai Z, Dai H, Pang B, Tong Z. Value of transthoracic echocardiography in therapy regimens evaluation in pulmonary embolism. J Thromb Thrombolysis. 2008 Dec;26(3):251-6. doi: 10.1007/s11239-007-0087-8. Epub 2007 Aug 21.
Results Reference
background
PubMed Identifier
19833628
Citation
Yang Wang, Chen Wang, Yuanhua Yang, Baosen Pang. Effect of recombinant single-chain urokinase-type plasminogen activator on experimental pulmonary embolism. Clin Appl Thromb Hemost. 2010 Oct;16(5):537-42. doi: 10.1177/1076029609343003. Epub 2009 Oct 14.
Results Reference
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Recombinant Streptokinase Versus Urokinase in Pulmonary Embolism in China (RESUPEC)

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