Examining the Feasibility of Using Pressure Gradient Regulated Automated Cerebral Spinal Fluid Drainage During External Lumbar Drain Trials
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The intellidrop device is an FDA-approved system that automates safe, small volume of cerebral spinal fluid drainage with continuous pressure monitoring, reducing nursing workload and human error while improving patient mobility and comfort
Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 99
Healthy Volunteers: f
View:
• All patients will be adults aged 60 years or older with suspected iNPH who are being admitted to the hospital for the purpose of an LDT specifically to evaluate for benefit from shunt placement.
Locations
United States
Texas
UT Southwestern Medical Center
RECRUITING
Dallas
Contact Information
Primary
Padraig O'Suilleabhain, M.D.
padraig.osuilleabhain@utsouthwestern.edu
214-648-2943
Backup
Maria Denbow, CCRP
maria.denbow@utsouthwestern.edu
214-648-6719
Time Frame
Start Date: 2026-05-14
Estimated Completion Date: 2026-10-31
Participants
Target number of participants: 10
Treatments
Experimental: Experimental - Intellidrop Automated CSF Drainage System
Device
Related Therapeutic Areas
Sponsors
Leads: University of Texas Southwestern Medical Center