Brain valve registry checks safety in 160 patients
NCT ID NCT05397106
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 160 people who have or will get a CODMAN CERTAS Plus valve, a device implanted in the brain to drain extra fluid. The main goal is to see if the valve is placed correctly and works without problems 30 days after surgery. Participants include children and adults with conditions like hydrocephalus, brain tumors, or stroke.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- CODMAN CERTAS Plus Programmable Valve (a surgically implanted device that helps drain excess fluid from the brain)
- What this could lead to
- If successful, this study will confirm that the valve is safe and works as intended for people with hydrocephalus.
- What could go wrong
- This is an observational registry, not a test of a new treatment. It only checks short-term device placement, not long-term benefits or risks.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AZ Delta - Roeselare
Roeselare, Belgium
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Canton Hospital St. Gallen
Sankt Gallen, Switzerland
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Freiburg University Hospital
Freiburg im Breisgau, Germany
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Heinrich Heine University, Dept of Neurosurgery, Universitätsklinik Düsseldorf
Düsseldorf, 40225, Germany
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Hospital12 de Octubre
Madrid, Spain
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Katharinenhospital - Neurochirurgische Klinik Stuttgart
Stuttgart, Germany
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Klinikum Dortmund Wirbelsäulenchirurgie
Dortmund, Germany
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University Hospital Leuven
Leuven, Belgium
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Universitätsklinikum Essen
Essen, Germany
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Other studies related to the condition(s) this trial covers.
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