Safety Study of the Angel™ Catheter in Subjects With Risk of Pulmonary Embolism

Bio2 Medical

Status and phase: Completed; Phase 1

Conditions: Venous Thromboembolism; Pulmonary Embolism; Deep Vein Thrombosis

Treatments: Device: Angel Catheter

Study type: Interventional

Funder types: Industry

Identifiers

NCT01403090

CPR-001

Details and patient eligibility

About

The Angel™ Catheter combines the functions of a vena cava filter and a multi-lumen central line catheter. The device is designed to be placed in the inferior vena cava via the femoral vein for the prevention of Pulmonary Embolism (PE) and for access to the central venous system. The primary endpoint is freedom from serious adverse events (SAE), defined as death, symptomatic pulmonary embolism or major bleeding .

Enrollment: 8 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Subject is 18 years and older

2. Be admitted to the hospital

   One of the following two criteria:

3. Patients with proven deep vein thrombosis (DVT) or pulmonary embolism ( PE), at high risk for pulmonary embolism and under consideration for insertion of a retrievable inferior vena cava (IVC) filter with at least one of the following criteria:

   • Contraindications for anticoagulation
   • Recurrent PE despite adequate anticoagulation
   • Emergency treatment following massive pulmonary embolism

4. Patients at high risk for developing PE who require but have a temporary or absolute contraindication for prophylaxis with anticoagulation, including:

   • Patients with multiple trauma and active or recent bleeding with contraindications to anticoagulation or that require a temporary stop of anticoagulation
   • severe head injury with coma
   • severe hemorrhagic stroke with coma
   • head injury with a long bone fracture
   • spinal cord injury with paraplegia or quadriplegia
   • multiple (≥2) long bone fractures with pelvic fracture
   • multiple (≥4) long bone fractures
   • Critically ill patients in the Medical or Surgical Intensive Care Unit with high risk of PE that require but are contraindicated for anticoagulation prophylaxis and will benefit from a temporary filter and a central venous access catheter
   • Patients who had recently undergone or are about to undergo a surgical procedure that requires temporary interruption of anticoagulation for Venous Thromboembolism (VTE) and will benefit from a temporary vena cava filter and central

Exclusion criteria

1. Patient is less than 18 years
2. Patient is pregnant or has a positive serum human chorionic gonadotropin (HCG) pregnancy test at baseline visit
3. Patient or next legal representative cannot give informed consent
4. Patients with anticipated survival < 2 days (catastrophic illness)
5. Body mass index greater than 35
6. Patient has a pre-existing filter
7. Participation in another simultaneous interventional medical investigation or interventional trial.
8. Patient has indications for a permanent filter at the time of the initial evaluation
9. Patient has an uncontrollable coagulopathy with active bleeding.
10. Patient with proven endocarditis or bacteremia
11. Patient has hypersensitivity to any of the components of the Angel™ Catheter, specifically Nitinol
12. Known acute or chronic thrombotic occlusion of both common femoral veins or iliac veins
13. Patient with functioning pelvic renal allograft on the only side available for device insertion
14. Patient who will undergo surgical procedure involving the femoral vein or pelvic veins through which the device must be inserted

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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8 participants in 1 patient group

Angel Catheter

Experimental group

Treatment:

Device: Angel Catheter