1400 Participants Needed

Data Collection for Pediatric Hydrocephalus

Recruiting at 15 trial locations
ML
Overseen ByMarcie Langley
Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: University of Utah
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to gather data on children with hydrocephalus, a condition characterized by excess fluid buildup in the brain. By collecting information on various surgeries and treatments for hydrocephalus, researchers aim to understand the condition's progression and the effectiveness of current treatments. The goal is to improve care and guide future research. Children who have undergone any type of neurosurgical procedure for hydrocephalus, such as shunt placements or endoscopic procedures, are suitable candidates for this trial.

As an unphased trial, this study offers participants a unique opportunity to contribute to the foundational understanding of hydrocephalus treatments, potentially improving future care for children.

Why are researchers excited about this trial?

Researchers are excited about the HCRN Core Data Project because it aims to better characterize patient populations within the Hydrocephalus Clinical Research Network. This trial isn't about testing a specific treatment; instead, it's about gathering vital data that could lead to more personalized and effective treatment approaches for hydrocephalus. By understanding the unique characteristics of different patient groups, researchers hope to improve current treatment strategies and outcomes, making care more tailored and potentially more effective for individuals with this condition.

Who Is on the Research Team?

JR

Jay Riva-Cambrin, MD

Principal Investigator

Alberta Children's Hospital

AK

Abhaya Kulkarni, MD, PhD

Principal Investigator

Sick Children's Hospital, Toronto, Ontario

TD

Tamara D Simon, MD, MSPH

Principal Investigator

University of Washington / Seattle Children's Hospital

RH

Richard Holubkov, Ph.D.

Principal Investigator

University of Utah

Are You a Good Fit for This Trial?

Inclusion Criteria

Subdural shunts
Ventriculoperitoneal shunt
Ventriculoatrial shunt
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection

Data about all neurosurgical hydrocephalus events is collected from the network Clinical Centers

Ongoing

Database Maintenance

Ongoing maintenance of the Core Data Project to understand variability, progression, and treatment practices

Lifetime of the HCRN

Follow-up

Participants are monitored for safety and effectiveness after data collection

4 weeks

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Utah

Lead Sponsor

Trials
1,169
Recruited
1,623,000+

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborator

Trials
1,403
Recruited
655,000+