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RECRUITING
NCT06097845
NA

Transcranial Ultrasound Via Sonolucent Cranioplasty

Sponsor: Northwell Health

View on ClinicalTrials.gov

Summary

Transcranial Ultrasound via Sonolucent Cranioplasty is a prospective, single arm, observational, open label (non-blinded) study to collect real world evidence on the use of transcranial ultrasound via sonolucent cranioplasty.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2023-06-27

Completion Date

2028-12-31

Last Updated

2025-09-15

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Transcranial Ultrasound

Patients who underwent reconstructive sonolucent cranioplasty will receive standard of care postoperative imaging (i.e. CT, MRI) in addition to ultrasound imaging. Ultrasound imaging will be performed by clinicians using FDA-approved ultrasound devices (GE Venue Go, Fujifilm Sonosite X-Porte, GE Volusion E10 and Clarius HD3 etc.) currently used in routine clinical practice.

Locations (1)

Lenox Hill Hospital

New York, New York, United States