Brain Blood Flow and Cerebral Autoregulation Monitoring in Critically Ill Children
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT07613918
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Cardiac Arrest
- Critical Illness
- Pediatric Critical Illness
- Respiratory Failure
- Traumatic Brain Injury
Eligibility Criteria
- Sex
- ALL
- Age
- 1 Day - 17 Years
- Healthy Volunteers
- Not accepted
Interventions
- Transcranial Doppler — DEVICETCD measurements synchronized to arterial blood pressure and ventilatory data, performed once daily for up to 5 days during PICU admission plus one additional pre-extubation scan if applicable, approximately 30 minutes each. Bilateral middle cerebral artery (MCA) insonation performed at each session.
Study Details
This study uses a non-invasive (external) ultrasound test called Transcranial Doppler (TCD) to measure how blood flows through the major arteries of the brain of children receiving care in the Pediatric Intensive Care Unit (PICU). TCD is already used for clinical reasons in many children, but it is not part of routine monitoring for every critically ill child. By using TCD, the investigators hope to better understand how brain blood flow changes during illness. They will also track children's functional status from before their illness to the time of PICU discharge to explore how brain blood flow patterns relate to neurological outcomes.125 participants will be enrolled and will be on study while in the PICU, estimated to be 3-14 days.
Key Dates
- Start date
- Jun 30, 2026
- Status verified
- Jun 2026
- Primary completion
- May 31, 2028
- Completion
- May 31, 2028
Study Design
- Enrollment
- 125 participants (estimated)
Arms
- Arm: PICU PatientsMechanically ventilated pediatric patients (1 day-17.5 years) admitted to the PICU.
Primary Outcome Measure
Change in Functional Status Scale (FSS) from baseline to PICU discharge [ Time Frame: Baseline FSS reflects pre-morbid functional status as reported by parents/guardians at enrollment; follow-up FSS assessed at PICU discharge (estimated 3-14 days) ]
Central Contacts
- Meg Baker
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| American Family Children's Hospital PICU | Madison | Wisconsin | 53792 | Talal Al Hendawi, MD (SUB_INVESTIGATOR) Neil Munjal, MD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Madison, WI
Related Studies
- Quality of Pediatric Resuscitation in a Multicenter CollaborativeRecruiting · Children's Hospital of Philadelphia · Los Angeles, California
- Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation ResearchRecruiting · Brain Inflammation Collaborative · Delafield, Wisconsin
- Clinical Effectiveness of the "PICU Up!" Multifaceted Early Mobility Intervention for Critically Ill ChildrenRecruiting · Johns Hopkins University · Madera, California
- Multi-Arm Multi-Stage Adaptive Platform Trial (APT) for the Acute Treatment of Traumatic Brain InjuryPHASE2 · Enrolling By Invitation · University of California, San Francisco · San Francisco, California