Rolling Meadows, ILNCT06086561Now EnrollingIRB Ready

Hydrocephalus Clinical Trial in Rolling Meadows, IL

Access cutting-edge hydrocephalus treatment through this clinical trial at a research site in Rolling Meadows. Study-provided care at no cost to qualified participants.

Sponsored by Rhaeos, Inc.

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Expert Care in Rolling Meadows

Access hydrocephalus specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hydrocephalus treatment provided free

Apply for This Rolling Meadows Location

Check if you qualify for this hydrocephalus clinical trial in Rolling Meadows, IL

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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 Rolling Meadows

    Convenient for IL 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 Rolling Meadows site if eligible
  4. 4Begin participation

About This Hydrocephalus Study in Rolling Meadows

This study evaluates the performance of a device for non-invasively assessing cerebrospinal fluid (CSF) shunt flow. Patients with an existing implanted shunt will wear the device to acquire longitudinal data.

Sponsor: Rhaeos, Inc.

Who Can Participate

Inclusion Criteria

At least one existing ventricular CSF shunt (functional or non-functional, including "virtual off" and ligated, orphaned, abandoned, tied-off, or fractured distal catheters)
Region(s) of intact skin overlying at least one unambiguously identifiable chronically indwelling ventricular shunt which crosses the clavicle and is appropriate in size for application of the study device
Available for remote and in-person follow-up during the 30-day measurement period (for subjects using the study device at home)
Subject is expected to remain in an inpatient setting for sufficient time to complete all required study device measurements (for subjects using the device in an inpatient hospital setting)
Signed informed consent by subject or a parent, legal guardian, health care agent, or surrogate decision maker (according to local statutes)
Subject or caregiver is able to clearly communicate and document information and shunt symptoms in English
Verbal assent by minors 12 years of age and older who are able to understand the study and communicate their decision
Patient is at least 5 years old but not more than 80 years old

Exclusion Criteria

Presence of an interfering open wound or edema over any portion of the shunt
Patient-reported history of adverse skin reactions to adhesives
Investigator judges that the subject is likely to be lost to follow-up due to unavailability or clinical outcome being unobtainable
Investigator judges that the subject is unlikely to successfully take reliable measurements at home (for subjects using the study device at home)
Investigator judges that the subject/subject's caretaker would not be able to successfully place the device without assistance
Use of the study device would interfere with standard patient care, or emergency surgery that cannot be delayed, or participation in the study will interfere with, or be detrimental to, administration of optimal healthcare to the subject
Participation in any other investigational procedural, pharmaceutical, and/or device study that may influence the collection of valid data under this study

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 Rolling Meadows?

Yes, this clinical trial (NCT06086561) has an active research site in Rolling Meadows, IL 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.

Hydrocephalus Treatment Options in Rolling Meadows, IL

If you're searching for hydrocephalus treatment options in Rolling Meadows, IL, this clinical trial (NCT06086561) 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 Rolling Meadows research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hydrocephalus 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 hydrocephalus clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Rolling Meadows, IL