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Epoprostenol in Pulmonary Embolism

Primary Purpose

Acute Pulmonary Embolism

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
epoprostenol
Sponsored by
Free University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Pulmonary Embolism focused on measuring pulmonary embolism, vasoconstriction, right ventricular dysfunction, epoprostenol, acute pulmonary embolism with right ventricular dysfunction

Eligibility Criteria

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

Inclusion Criteria:

  • acute (symptoms <24 hrs) with right ventricular dilatation (>30 mm end diastolic, systolic PAP > 50 mmHg,
  • absence of right ventricular wall hypertrophy)

Exclusion Criteria:

  • age below 18 years or above 70 years
  • body mass index >35 kg/m2
  • duration of symptoms >24 hours (since onset or acute increase in symptoms)
  • severe circulatory shock (systemic blood pressure systolic <80 mmHg, or diastolic blood pressure <45 mmHg) or respiratory failure, requiring mechanical ventilation.
  • patients who, in the opinion of the supervising physician, require thrombolytic therapy.
  • severe pre-existent cardiopulmonary disease (heart failure, obstructive pulmonary disease, emphysema)
  • atrial fibrillation
  • refusal or inability to give informed consent

Sites / Locations

  • Free University Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

epoprostenol intraveneously

Arm Description

epoprostenol iv versus placebo iv, both on top of low molecular weight heparin

Outcomes

Primary Outcome Measures

Right ventricular end diastolic diameter (ultrasound)

Secondary Outcome Measures

systolic pulmonary artery pressure (ultrasound)

Full Information

First Posted
November 13, 2009
Last Updated
November 13, 2009
Sponsor
Free University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01014156
Brief Title
Epoprostenol in Pulmonary Embolism
Official Title
Effects of Intravenous Epoprostenol Sodium (Flolan®) in Patients With Moderate-to-Severe Pulmonary Thrombo-Embolism
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
June 2006 (Actual)
Study Completion Date
June 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Free University Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
You are admitted to hospital because of pulmonary embolism. You are treated with anticoagulants. The investigators know that, despite this treatment, pulmonary embolism can be a threat especially if heart function is compromized. The investigators investigate a well known study drug (epoprostenol) on top of regular treatment with anticoagulants, to see if heart function can be optimized
Detailed Description
Pulmonary thromboembolism (PE) with circulatory and/or respiratory symptoms is associated with high morbidity and mortality. Acute pulmonary hypertension is the hallmark of severe PE, and is to be held responsible for the full spectrum of clinical manifestations and complications. Although it is common belief that only mechanical obstruction by thrombus mass causes this pulmonary hypertension, there is strong evidence indicating that pulmonary vasoconstriction contributes significantly to the rise in pulmonary vascular resistance. Although all patients will receive anticoagulant treatment immediately after the diagnosis is established, morbidity and mortality are still disturbingly high when circulatory and/or respiratory symptoms accompany PE, or when hemodynamically stable PE patients have echocardiographic signs of acute right ventricle overload. There are no generally accepted guidelines for additional treatment options in these patients with moderate-to-severe PE. Thrombolytic therapy is recommended by many when hemodynamic symptoms are severe, but its effectiveness has never been proven in a controlled trial. In patients with moderate-to-large PE associated with echocardiographic signs of right ventricle overload, but who are still circulatory stable, mortality is increased, but thrombolytic therapy appears not to be beneficial. Given the plausible role of pulmonary vasoconstriction in the pathogenesis of PE associated pulmonary hypertension, the potential benefit of pulmonary vasodilators is important.There is experimental evidence that antagonising pulmonary vasoconstriction by the administration of selective vasodilators may be beneficial in animals with PE. In addition, anecdotal evidence of a similar kind exists for humans with acute PE. We hypothesise that in PE patients who have echocardiographic evidence of acute right ventricle overload, epoprostenol sodium (Flolan®) results in partial or complete reversal of echocardiographic abnormalities, as well as in improvement in respiratory and circulatory symptoms and signs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Pulmonary Embolism
Keywords
pulmonary embolism, vasoconstriction, right ventricular dysfunction, epoprostenol, acute pulmonary embolism with right ventricular dysfunction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
epoprostenol intraveneously
Arm Type
Experimental
Arm Description
epoprostenol iv versus placebo iv, both on top of low molecular weight heparin
Intervention Type
Drug
Intervention Name(s)
epoprostenol
Other Intervention Name(s)
prostacyclin, flolan
Intervention Description
titration up to 4 ng/kg/min
Primary Outcome Measure Information:
Title
Right ventricular end diastolic diameter (ultrasound)
Time Frame
0, 2,5 4, 24 and 72 hours
Secondary Outcome Measure Information:
Title
systolic pulmonary artery pressure (ultrasound)
Time Frame
identical to primary measure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: acute (symptoms <24 hrs) with right ventricular dilatation (>30 mm end diastolic, systolic PAP > 50 mmHg, absence of right ventricular wall hypertrophy) Exclusion Criteria: age below 18 years or above 70 years body mass index >35 kg/m2 duration of symptoms >24 hours (since onset or acute increase in symptoms) severe circulatory shock (systemic blood pressure systolic <80 mmHg, or diastolic blood pressure <45 mmHg) or respiratory failure, requiring mechanical ventilation. patients who, in the opinion of the supervising physician, require thrombolytic therapy. severe pre-existent cardiopulmonary disease (heart failure, obstructive pulmonary disease, emphysema) atrial fibrillation refusal or inability to give informed consent
Facility Information:
Facility Name
Free University Medical Center
City
Amsterdam
ZIP/Postal Code
1081 HV
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
20353588
Citation
Kooter AJ, Ijzerman RG, Kamp O, Boonstra AB, Smulders YM. No effect of epoprostenol on right ventricular diameter in patients with acute pulmonary embolism: a randomized controlled trial. BMC Pulm Med. 2010 Mar 30;10:18. doi: 10.1186/1471-2466-10-18.
Results Reference
derived

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Epoprostenol in Pulmonary Embolism

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