Percutaneous Embolectomy, Ultrasound Assisted Thrombolysis or Heparin for Intermediate High Risk Pulmonary Embolism

NCT ID: NCT06453876

Last Updated: 2025-04-04

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 210 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-06-01
• Study Completion Date: 2029-10-31

Brief Summary

The STRATIFY II trial investigates the efficacy of three different approaches to reducing thrombus burdon in patients with acute intermediate high-risk pulmonary embolism: percutaneous embolectomy (the Flow Triever® system, INARI medical), USAT (EKOS® system, Boston Scientific with low dose alteplase) and heparin with the option to perform full-dose thrombolysis. As a co-primary secondary end point the trial assess the incremental efficacy of the embolectomy vs the catheter based low dose thrombolysis approach.

Thus the two main hypothesis being tested are:

1. Thrombus burden reduction after 48-96 h is increased with a catheter based (embolectomy or USAT) compared to the a heparin with optional high dose thrombolysis approach (1st co-primary outcome)

2. Thrombus burden reduction after 48-96 h is increased with percutaneous embolectomy compared to USAT with low-dose alteplase (2nd co-primary outcome)

Detailed Description

BACKGROUND Intermediate high-risk PE is associated with an up to 10% risk of death even if the circulations of the patient is only marginally impacted (1). Full dose thrombolysis has been investigated is two randomized trials but finding the intervention to be efficacious in preventing hemodynamic deterioration, but at the cost of an increased risk og bleeding with cancels the benefit of thrombolysis with regards to risk of death (2, 3). Therefore recent guidelines suggest that patients are managed by heparins with thrombolysis available as a rescue therapy if the patient deteriorates hemodynamically (1). Further two small clinical have trials have investigated the role of low dose thrombolysis finding a substantial reduction in late incidence of pulmonary hypertension (4) and similar efficacy of half dose thrombolysis and lower occurrence of bleeding compared to full doses thrombolysis (5).

Since then catheter based interventions for administering low Thrombolysis for acute PE has been introduced. Some interventionalists use simple catheters while the EKOS® system of USAT claims to increase the efficacy of thrombolytics by applying a mechanical force from ultrasound emitting crystals nead the emboli while slowly administering the thrombolytics near the thrombus in the pulmonary arteries. The USAT techniques has been tested in a small randomized trial, finding the treatment to efficacious in terms of reducing right heart dilatation (6). Later a dose finding RCT should similar efficacy of dosages of alteplase in USAT ranging from 4 mg to 24 mg per catheter (7). The HI-PEITHO trial (NCT04790370) is a 406 patient trial current enrolling patients, and the STRATIFY trial from our group (NCT04088292) is a 210 patient trial also currently including patients, and thus more knowledge of the efficacy of this approach will be available in 1-2 years.

Recently catheter-based embolectomy has been introduced. While no randomized trials have compared this technique to the guidelines supported strategy of UFH or LMWH, several registries and sace series have been put forward, suggesting a significant efficacy and a acceptable risk of bleeding. The INARI FlowTriever system ® has been use in a substantial number of patients, but have only been reported in none peer-reviewed presentation as results of two registries comparing patients treated with percutaneous embolectomy and a registry describing 'real world data' has been presented online (8) and in comment section in medical journals (9). An ongoing randomized trial comparing percutaneous embolectomy and catheter directed thrombolysis, is currently recruiting patients (NCT05111613)(10) and another comparing embolectomy and heparins is planned (NCT06055920).

Balancing the risk and efficacy of the treatment strategy remains important and since a lack of data both proving the efficacy of the novel treatment alternatives and limited data comparing efficacy in trial with a suitable design, a clinical equipoise remains.

TRIAL OBJECTIVES AND HYPOTHESIS The STRATIFY II trial investigates the efficacy of three different approaches to reducing thrombus burdon in patients with acute intermediate high-risk pulmonary embolism: percutaneous embolectomy (the Flow Triever® system, INARI medical), USAT (EKOS® system, Boston Scientific with low dose alteplase) and heparin with the option to perform full-dose thrombolysis. As a co-primary secondary end point the trial assess the incremental efficacy of the embolectomy vs the catheter based low dose thrombolysis approach.

Thus the two main hypothesis being tested are:

1. Thrombus burden reduction after 48-96 h is increased with a catheter based (embolectomy or USAT) compared to the a heparin with optional high dose thrombolysis approach (1st co-primary outcome)

2. Thrombus burden reduction after 48-96 h is increased with percutaneous embolectomy compared to USAT with low-dose alteplase (2nd co-primary outcome) SETTING AND PATIENT POPULATION SETTING The trial is including patients diagnosed with an acute PE (defined as symptom duration of less than 14 days) with intermediate- high risk , please see section of definition below. Patients are recruited from participating centers by the attending cardiologist, either in the emergency room or at the ward. Since risk stratification most often involves a cardiologist the investigators expect the majority of patients to be included in the trial immediately after risk stratification.

The participants will be informed on the possible inclusion in the trial in the ward, and every measure possible will be taken to ensure a quit environment for the information. The patient will be informed about their right to have an assessor present during the information session, and that they may take the time needed to consider their participation in the trial and giving their informed consent. The informed consent will be obtained soon after the patient have been informed on their diagnosis of intermediate-high risk PE.

DEFINITIONS Definition of Intermedidate- high risk PE is based on ESC guideline classification from 2019 (1) as identification of PE in the pulmonary main trunk, main and segmental pulmonary arteries on CT angiography performed as part of the diagnostic work-up of patients with clinical suspicion of acute PE RV dysfunction is defined as

• RV/LV ratio of > 1 on CT angiography or echocardiography (apical 4 chamber view in-diastole) OR
• RV systolic function by visual assessment or TAPSE < 18 mm OR
• TR gradient > 40 mmHg Elevated Cardiac Biomarker
• Increase in cardiac Troponins (I or T) above normal OR
• Increase Creatine Kinase MB (CKMB) above normal OR
• Increase in NT-pro-BNP above normal In the absence of shock at time of screening defined as
• Systolic blood pressure > 100 mmHg INCLUSION CRITERIA

1. Age ≥ 18 years

2. Informed consent for trial participation

3. Intermediate high-risk PE according to ESC criteria

4. Thrombus visible in main, lobar or segmental pulmonary arteries on CT angiography

5. 14 days of symptoms or less EXCLUSION CRITERIA

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1. Altered mental state (GCS < 14)

2. No qualifying CT angiography performed (> 24 hour since CT angiography)

3. Females of child bearing potential, unless negative HCG test is present

4. Thrombolysis for PE within 14 days of randomization

5. Thrombus passing through patent Foramen Ovale (risk of paradoxical embolism)

6. Ongoing oral anticoagulation therapy (heparins, aspirin, antiplatelet therapy and NOAC allowed)

7. Comorbidity making 6 months survival unlikely

8. Absolute contraindications for thrombolysis

1. Hemorrhagic stroke or stroke of unknown origin at any time

2. Ischemic stroke in the preceding 6 months

3. Central nervous system damage or neoplasms

4. Recent major trauma/surgery/head injury in the preceding 3 weeks

5. Gastrointestinal bleeding within the last month

6. Known bleeding risk Relative contraindications do not preclude randomization. Relative contraindications include: Transient ischemic attack in the preceding 6 months, Oral anticoagulant therapy, Pregnancy, or within one week post partum, Non-compressible puncture site, Traumatic resuscitation, Refractory hypertension (systolic blood pressure >180 mm Hg), Advanced liver disease, Infective endocarditis, Active peptic ulcer OUTCOMES CO-PRIMARY ENDPOINT

• Reduction in modified Miller score (score of thrombus involvement and segmental flow)(11, 12) comparing percutaneous treated groups (embolectomy and USAT combined) to heparin/LMWH group, p<0.01 (n=140 vs. n=70).
• Reduction in modified Miller score (score of thrombus involvement and segmental flow)(11, 12) comparing percutaneous embolectomy and USAT, p<0.04 (n=70 vs n=70) SECONDARY ENDPOINTS
• • Bleeding complications (major and minor bleeding complication according to the Thrombolysis in Myocardial Infarction classification)
• Duration of index admission, including hospital-based rehabilitation
• Dyspnoea index (Visual analogue scale) after 48-96 h and after 3 months
• FiO2, blood pressure, and respiratory rate, heart rate at time of follow-up CTPA
• Mortality in the three groups (log-rank), and hazard ratio in multivariable analysis using the UFH/LMWH as a reference
• Incidence of TR gradient > 40 mmHg at 3 months follow-up echocardiography
• 6MWT at 3 months follow up comparing the three groups
• Quality of life at 3 months follow-up comparing the three groups (PEmb-Qol and 5Q-5D-5L)

Conditions

Pulmonary Embolism

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Unfractionated Heparin / Low molecular heparin and thrombolysis if needed

Standard medical Therapy for intermediate-high risk pulmonary embolism

Group Type: ACTIVE_COMPARATOR

Heparin

Intervention Type: DRUG

Active comparator

Ultrasound assisted Thrombolysis

Ultrasound assisted Thrombolysis using teh EKOS system. 10 mg af alteplase over 6 hours total and heparin

Group Type: ACTIVE_COMPARATOR

Ultrasound assisted Thrombolysis

Intervention Type: DEVICE

Please see Arms

Percutaneous Thrombectomy

Percutaneous Embolectomy using the Inari (R) Flowtriever thrombectomy system (R) and heparin

Group Type: ACTIVE_COMPARATOR

Percutaneous Embolectomy

Intervention Type: DEVICE

Please see arms

Interventions

Ultrasound assisted Thrombolysis

Please see Arms

Intervention Type: DEVICE

Percutaneous Embolectomy

Please see arms

Intervention Type: DEVICE

Heparin

Active comparator

Intervention Type: DRUG

Other Intervention Names

EKOS system; Inari FlowTriever; Unfractionated or low molecular weight heparin

Eligibility Criteria

Inclusion Criteria

1. Age ≥ 18 years

2. Informed consent for trial participation

3. Intermediate high-risk PE according to ESC criteria

4. Thrombus visible in main, lobar or segmental pulmonary arteries on CT angiography

5. 14 days of symptoms or less

Exclusion Criteria

1. Altered mental state (GCS < 14)

2. No qualifying CT angiography performed (> 24 hour since CT angiography)

3. Females of child bearing potential, unless negative HCG test is present

4. Thrombolysis for PE within 14 days of randomization

5. Thrombus passing through patent Foramen Ovale (risk of paradoxical embolism)

6. Ongoing oral anticoagulation therapy (heparins, aspirin, antiplatelet therapy and NOAC allowed)

7. Comorbidity making 6 months survival unlikely

8. Absolute contraindications for thrombolysis

1. Hemorrhagic stroke or stroke of unknown origin at any time

2. Ischemic stroke in the preceding 6 months

3. Central nervous system damage or neoplasms

4. Recent major trauma/surgery/head injury in the preceding 3 weeks

5. Gastrointestinal bleeding within the last month

6. Known bleeding risk Relative contraindications do not preclude randomization. Relative contraindications include: Transient ischemic attack in the preceding 6 months, Oral anticoagulant therapy, Pregnancy, or within one week post partum, Non-compressible puncture site, Traumatic resuscitation, Refractory hypertension (systolic blood pressure >180 mm Hg), Advanced liver disease, Infective endocarditis, Active peptic ulcer

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Zealand University Hospital

OTHER

Sponsor Role: collaborator

Copenhagen University Hospital at Herlev

OTHER

Sponsor Role: collaborator

Jesper Kjaergaard

OTHER

Sponsor Role: lead

Responsible Party

Jesper Kjaergaard

Consultant MD PhD DMSc

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

Copenhagen University Hospital Gentofte

Gentofte Municipality, Capital Region, Denmark

Copenhagen University Hospital Bispebjerg Hospital

Bispebjerg, , Denmark

Copenhagen University Hospital Rigshospitalet

Copenhagen, , Denmark

Copenhagen University Hospital, Herlev Gentofte Hospital

Herlev, , Denmark

Countries

Denmark

Central Contacts

Jesper Kjaergaard, MD PhD DMSc

Role: CONTACT

jesper.kjaergaard.05@regionh.dk

+4535450969

Lia Bang, MD PhD

Role: CONTACT

lia.evi.bang@regionh.dk

+4535450988

Other Identifiers

STRATIFY-II 1.0 (04OCT2023)

Identifier Type: -

Identifier Source: org_study_id