X-Ray Verified Accuracy of the proGAV Verification Instrument

Aesculap, Inc.12 enrolled

Overview

This study is to verify the use of a hand held tool to verify the new setting of a hydrocephalus shunt (proGAV). This tool would be used in place of an Xray of the patient's head, which is how settings are verified currently.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Hydrocephalus Shunt (proGAV) Requiring Adjustment

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Implanted with proGAV Requiring adjustment Implant must be palpable under the skin Exclusion Criteria: * Unwilling to consent Implanted within 7 days of inclusion visit

Locations (2)

Valley Children's Hospital

Madeira, California, United States

Geisinger Medical Center

Danville, Pennsylvania, United States

Outcomes

Primary Outcomes

Level of agreement between the proGAV® verification instrument measurement and X-ray control measurements.

Time frame: 1day

Data from ClinicalTrials.gov

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