Clinical Trial

Examining the Feasibility of Using Pressure Gradient Regulated Automated Cerebral Spinal Fluid Drainage During External Lumbar Drain Trials

Study acronym: UPGRADE
Recruiting
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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
Protocol Amendment History 1 change
critical Recruitment opened 2026-06-03
Trial Details
NCT Number NCT07494812
Lead Sponsor University of Texas Southwestern Medical Center
Conditions NPH (Normal Pressure Hydrocephalus)
Enrollment 10 participants
Start Date 2026-05-14
Primary Completion 2026-10-31 (estimated)
Study Completion 2026-10-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-02