A Study on the Safety of Hakim Programmable Shunt System

Status Completed

Clinical Trial Summary

This study aimed to collect safety information from subjects implanted with a shunt system (trade name: Hakim Shunt Programmable System) produced by Codman & Shurtleff, Inc. of the United States. Device safety would be assessed based on all the adverse events that occurred within one year after the subjects implanted the catheter.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Hydrocephalus

Clinical Trial Details

NCT number	NCT04285489
Study type	Observational
Source	Integra LifeSciences Corporation
Contact
Status	Completed
Phase
Start date	May 2, 2020
Completion date	July 28, 2020

View Details

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