Orange, CANCT05701917Now EnrollingIRB Ready

Venous Thromboembolism Clinical Trial in Orange, CA

Access cutting-edge venous thromboembolism treatment through this clinical trial at a research site in Orange. Study-provided care at no cost to qualified participants.

Sponsored by Inari Medical

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Expert Care in Orange

Access venous thromboembolism specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related venous thromboembolism treatment provided free

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Check if you qualify for this venous thromboembolism clinical trial in Orange, CA

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Why Participate?

  • No-Cost Study Care

  • Local to Orange

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Orange site if eligible
  4. 4Begin participation

About This Venous Thromboembolism Study in Orange

This study is a prospective, multicenter, randomized controlled trial of an interventional strategy using the ClotTriever System to achieve and maintain vessel patency (ClotTriever Intervention Arm) versus conservative medical management using anticoagulation therapy alone (Conservative Medical Management Arm) in the treatment of subjects with symptomatic unilateral iliofemoral DVT. The study will collect data on demographics, comorbidities, details from the DVT diagnosis and treatment, and clinical outcomes through the 6-month follow up visit.

Sponsor: Inari Medical

Who Can Participate

Inclusion Criteria

Age ≥ 18 years
Proximal lower extremity unilateral DVT involving at least the common femoral, external iliac, or common iliac veins, alone or in combination
Symptom onset within 12 weeks of enrollment in the study
Significant symptoms, as defined by a Villalta score \> 9
Willing and able to provide informed consent

Exclusion Criteria

Bilateral iliofemoral DVT
Prior venous stent in the target venous segment
IVC aplasia/hypoplasia or other congenital anatomic anomalies of the IVC or iliac veins
IVC filter in place at the time of enrollment
Limb-threatening circulatory compromise (e.g., phlegmasia)
Clot in transit including IVC thrombus presenting as extension of \>2cm into the IVC from the CIV
Symptomatic PE with right heart strain where the physician judges that a DVT intervention is inappropriate at this time.
Inability to be a candidate for intervention due to medical or technical reasons based on physician judgement
Severe allergy, hypersensitivity to, or thrombocytopenia from heparin
Severe allergy to iodinated contrast agents that cannot be mitigated
Hemoglobin \< 8.0 g/dL, INR \> 1.7 before warfarin was started, or platelets \< 50,000/µl which cannot be corrected prior to enrollment
Severe renal impairment (estimated GFR \< 30 ml/min) in patients who are not yet on dialysis
Inability to provide therapeutic anticoagulation per Investigator discretion
Uncontrolled severe hypertension on repeated readings (systolic \> 180mmHg or diastolic \> 105mmHg)
Recently (\< 30 days) had DVT interventional procedure
Subject is participating in another study that may interfere with this study
Life expectancy \< 6 months or chronic non-ambulatory status
Known hypercoagulable states that, in the opinion of the Investigator, cannot be medically managed throughout the study period
Subject has any condition for which, in the opinion of the Investigator, participation would not be in the best interest of the subject (e.g., contraindication to use of ClotTriever per local approved labeling, compromise the well-being or that could prevent, limit, or confound the protocol-specified assessments)
Subject has previously completed or withdrawn from this study
Patient unwilling or unable to conduct the follow up visits per protocol

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Orange?

Yes, this clinical trial (NCT05701917) has an active research site in Orange, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Venous Thromboembolism Treatment Options in Orange, CA

If you're searching for venous thromboembolism treatment options in Orange, CA, this clinical trial (NCT05701917) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Orange research site is actively enrolling participants for this clinical trial. You'll receive care from experienced venous thromboembolism specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all venous thromboembolism clinical trials near you to find additional studies recruiting in your area.

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