Recruiting

Securement Device

Sponsor:

University of Colorado, Denver

Code:

NCT04462861

Conditions

Central Venous Catheter Exit Site Infection

Central Venous Catheter Related Bloodstream Infection

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Not accepted

Interventions

Central venous access device (CVAD) Snuggie Securement Device

Study Details

Brief summary:

An external tunneled central venous access device (CVAD) is a small plastic tube that is tunneled under the skin into a major vein for long-term use (Figure 1). Patients who require a tunneled CVAD are some of the sickest patients we encounter and include oncology, hematology, and gastrointestinal (intestinal failure) patients. These patients are heavily reliant on their tunneled CVAD, which can be a lifeline for long-term administration of chemotherapeutics, IV medications, blood product transfusions, antibiotics, enteral nutrition, blood draws and fluids. Unfortunately, nearly 30% of pediatric external tunneled CVADs fail prior to the completion of treatment. External tunneled CVAD failures lead to unnecessary morbidity and mortality, interruption of medical therapy, and the added costs and risks associated with additional procedural complications. It is hypothesized that a newly designed securement method for external tunneled central venous access devices (CVAD) will reduce catheter-related complications and increase patient, parent and provider satisfaction, compared to the current standard of care, which is a clear transparent film dressing over the catheter exit site. A 20 patient, prospective clinical trial is proposed to address the following specific aims, which will determine if the securement device:

1. Is rated by patients, parents and providers as easy to apply and comfortable for users
2. Reduces CVAD-related complications, such as delayed healing of the tract, catheter-related infections, and episodes of catheter dislodgement
3. Improves the quality of life for patients and their parents
4. Is preferred over the standard, clear transparent dressing alone
5. Requires any design modifications to improve performance and/or comfort of the device

Conditions

Central Venous Catheter Exit Site Infection

Central Venous Catheter Related Bloodstream Infection

Study ID

NCT04462861

Start date

Oct 19, 2020

Status verified date

Jun, 2023

Completion date

Jun, 2024

Anticipated

Primary completion date

Jun, 2024

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patients aged 31 days to 18 years old, who will undergo surgical placement of a tunneled CVAD
  • Any patient with a pre-existing CVAD, who presents to the surgery clinic, emergency department, or is seen as an inpatient consult relating to complications associated with their CVAD
  • Patients admitted to the hospital with a pre-existing CVAD for reasons unrelated to the CVAD will be eligible for the study

Exclusion Criteria:

  • Any assenting child or consenting parent/guardian can at any time refuse to participate in the study and will be removed
  • Any patient whose parents or legal guardians cannot be reached in person or by telephone to provide consent
  • Any prisoners, pregnant women, or person with impaired decision-making capacity

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: CVAD securement device

Patients with a pre-existing CVAD who will trial the new securement dressing

Interventions

Central venous access device (CVAD) Snuggie Securement Device

Participants will be given a prototype of a CVAD securement device for a three week trial. Descriptive data relating to user satisfaction will be collected at 1 and 3 weeks

Primary outcome measure

  • Comfort [ Time Frame: 3 weeks ]
  • quality of materials [ Time Frame: 3 weeks ]
  • Quality of Adhesive [ Time Frame: 3 weeks ]
  • Ease of use [ Time Frame: 3 weeks ]
  • Skin irritation [ Time Frame: 3 weeks ]
  • Infection [ Time Frame: 3 weeks ]
  • dislodgement [ Time Frame: 3 weeks ]
  • catheter breakage [ Time Frame: 3 weeks ]
  • types and numbers of interactions with healthcare providers [ Time Frame: 3 weeks ]
  • Perceived safety [ Time Frame: 3 weeks ]
  • overall impression [ Time Frame: 3 weeks ]

Central Contacts and Locations

Locations

Children's Hospital Colorado

Recruiting

Aurora, Colorado, United States, 54008

Contacts

Marina Reppucci, MD

203-731-4914

More Information

Sponsor

University of Colorado, Denver

Last update posted

Jun 15, 2023

Last verified

Jun, 2023

Keywords

  • central venous access device, CVAD

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Colorado, Denver on 2023-06-15.