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Study identifier: NCT05649904 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

AFFECT Study for Patients With Intraventricular Hemorrhage, Subarachnoid Hemorrhage, Subdural Hematoma, and Ventriculitis

Condition: Intraventricular Hemorrhage · Subarachnoid Hemorrhage · Subdural Hematoma  ·  Sponsor: Ohio State University

PhaseNA
Planned participants240
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate efficacy and safety of evacuation of cerebrospinal fluid, blood, and harmful bacteria from the intraventricular, subdural and subarachnoid spaces by Active Controlled Irrigation and Drainage (IRRAflow) compared to Passive External Ventricular Drainage (EVD). Subjects with intraventricular hemorrhage, subarachnoid hemorrhage, subdural bleeding, and ventriculitis will be randomized to receive the IRRAflow device or EVD device and followed for one month post-procedure to compare outcomes between the subject groups.

This description comes directly from the study's public registry record.

Talk to the study team

Edouard Beliaire  ·  6143666936  ·  edouard.belizaire@osumc.edu

Patrick Youssef, MD  ·  6143666590  ·  patrick.youssef@osumc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

The Ohio State University Wexner Medical CenterColumbus, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05649904