New collagen patch tested for brain surgery repair
NCT ID NCT07217132
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is monitoring the safety and performance of a collagen membrane used to repair the dura mater, the protective lining of the brain, after surgery. About 54 adults who need this type of repair will be enrolled. Doctors will track any complications and rate how well the product handles and performs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Collagen Dura Membrane - Suturable (DMS)
- What this could lead to
- If successful, this study could confirm that this collagen membrane is a safe and easy-to-use option for repairing the brain's protective covering during surgery.
- What could go wrong
- This is a small, early-stage monitoring study with only 54 participants and no comparison group, so results may not apply to everyone. There is also a risk of allergic reaction in people sensitive to cow-derived materials.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 54 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The general population will be included in the study where a dura substitute is required for the repair of dura mater.
- Ages
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18 years and older
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with a dural defect requiring repair with a dural substitute * Patient is 18 years or older * Patient of child-bearing potential is not pregnant or nursing Exclusion Criteria: * Patients with a known history of hypersensitivity to bovine derived materials * Patients that are non-English speaking * Subjects requiring Legally Authorized Representative
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Baptist Health South Florida
Miami, Florida, 33176, United States
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