Columbus, OHNCT05879835Now EnrollingIRB Ready

Pediatric Intestinal Failure Clinical Trial in Columbus, OH

Access cutting-edge pediatric intestinal failure treatment through this clinical trial at a research site in Columbus. Study-provided care at no cost to qualified participants.

Sponsored by SterileCare Inc.

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Expert Care in Columbus

Access pediatric intestinal failure specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related pediatric intestinal failure treatment provided free

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Check if you qualify for this pediatric intestinal failure clinical trial in Columbus, OH

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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 Columbus

    Convenient for OH 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 Columbus site if eligible
  4. 4Begin participation

About This Pediatric Intestinal Failure Study in Columbus

A multi-site, randomized, 2-arm open-label trial to determine if 4% Tetrasodium (EDTA) catheter lock solution is more effective than heparin lock (standard of care) in preventing central venous catheter occlusions in children with intestinal failure (IF) on total parenteral nutrition (TPN).

Sponsor: SterileCare Inc.

Who Can Participate

Inclusion Criteria

Patients managed by the intestinal rehabilitation program at one of the participating centers.
Diagnosis of intestinal failure defined as need for PN support for \>60 days in previous 74 days for primary intestinal disease (short bowel syndrome, primary motility disorder, mucosal enteropathy).
Expectation of the treating physician that the patient will require PN for at least 6 months following enrollment.
Age less than 18 years at diagnosis but greater than 4 weeks chronological age or 40 weeks estimated gestational age, whichever is greater.
Stable TPN cycling (4 hours off TPN minimum per day) enabling home TPN management
Presence of a tunneled central venous catheter (CVC), port-a-catheter, or peripherally inserted central catheter (PICC).
Clinical stability for at least 4 weeks and no acute medical comorbidities.
A minimum dwell time of 4 consecutive hours daily.
Care provider willing to provide informed consent to participate in the trial and willing to comply with randomization and study protocol.

Exclusion Criteria

A temporary CVC (jugular or femoral) or peripheral catheter.
Patients receiving long-term PN, but not due to a primary intestinal disorder (i.e., oncology patients or premature neonates on PN due to intestinal immaturity).
Known hypersensitivity, allergy, or reaction to EDTA.
Pregnancy or nursing mother.
Participation in another investigational device or drug trial within 30 days prior to enrollment (unless approved by the principal investigators of the trial).
Severe coagulopathy (platelets \<50,000, or INR \> 1.5).
Diagnosis of immunodeficiency disorder.
Unstable medical condition requiring hospital admission
Received antibiotic therapy for CLABSI within last 14 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 Columbus?

Yes, this clinical trial (NCT05879835) has an active research site in Columbus, OH 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.

Pediatric Intestinal Failure Treatment Options in Columbus, OH

If you're searching for pediatric intestinal failure treatment options in Columbus, OH, this clinical trial (NCT05879835) 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 Columbus research site is actively enrolling participants for this clinical trial. You'll receive care from experienced pediatric intestinal failure 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 pediatric intestinal failure clinical trials near you to find additional studies recruiting in your area.

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