New York, NYNCT06418282Now EnrollingIRB Ready

Phlebolymphedema Clinical Trial in New York, NY

Access cutting-edge phlebolymphedema treatment through this clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by Koya Medical, Inc.

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Expert Care in New York

Access phlebolymphedema specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related phlebolymphedema treatment provided free

Apply for This New York Location

Check if you qualify for this phlebolymphedema clinical trial in New York, NY

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY 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 New York site if eligible
  4. 4Begin participation

About This Phlebolymphedema Study in New York

An open-label, multi-center, prospective VA study to evaluate the effectiveness and health economics of a Novel Portable Non-Pneumatic Active Compression Device (NPCD) for lymphedema/phlebolymphedema

Sponsor: Koya Medical, Inc.

Who Can Participate

Inclusion Criteria

Males and females ≥ 18 years of age
Capable and willing to sign the informed consent and deemed capable of following the study protocol
Subjects must have a diagnosis of unilateral or bilateral lower extremity edema or lower extremity lymphedema/phlebolymphedema as a consequence of chronic venous insufficiency
Subjects who have medical clearance using diagnostic confirmation through venous duplex to rule out DVT and superficial/deep reflux

Exclusion Criteria

Inability or unwillingness to participate in all aspects of study protocol and/or inability to provide informed consent
Individuals with a history or presence of a systemic disorder or condition that could place the subject at increased risk from sequential compression therapy
Subjects must not have any diagnosed cognitive or physical impairment that would interfere with the use of the device
Non-ambulatory individuals
Female: BMI \> 34 (5'4", 200 lbs.)
Male: BMI \> 34 (5'9", 230 lbs.)
(Max circumference at patella 58 cm; Max circumference at gluteal fold 75 cm)
Diagnosis of lipedema
Diagnosis of active or recurrent cancer (\< 3 months since completion of chemotherapy, radiation therapy or primary surgery for the cancer)
Diagnosis of acute infection (in the last four weeks)
Diagnosis of active/open wound/ulcer
Diagnosis of acute thrombophlebitis (in last 2 months)
Diagnosis of pulmonary embolism or deep vein thrombosis within the previous 6 months
Diagnosis of pulmonary edema
Diagnosis of congestive heart failure (uncontrolled/uncompensated)
Diagnosis of chronic kidney disease with acute renal failure
Diagnosis of epilepsy
Subjects with poorly controlled asthma
Any condition where increased venous and lymphatic return is undesirable
Women who are pregnant, planning a pregnancy or nursing at study entry
Participation in any clinical trial of an investigational substance or device during the past 30 days

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 New York?

Yes, this clinical trial (NCT06418282) has an active research site in New York, NY 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.

Phlebolymphedema Treatment Options in New York, NY

If you're searching for phlebolymphedema treatment options in New York, NY, this clinical trial (NCT06418282) 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 New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced phlebolymphedema 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 phlebolymphedema clinical trials near you to find additional studies recruiting in your area.

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