MiDura-Study (Neuro-Patch in Duraplasty) (MiDura)

  • End date
    Jan 16, 2026
  • participants needed
  • sponsor
    Aesculap AG
Updated on 16 June 2022


The aim of this study is to collect systematically and proactively data regarding the performance of Neuro-Patch, like complications and handling, under daily clinical practice when used as intended by the manufacturer

Condition Meningioma, Tumor, Brain, Chiari Malformation, Vascular Malformation, Hydrocephalus, Tethered Cord, Dural Fistula, Craniotomy, Spinal Surgery, Duraplasty
Clinical Study IdentifierNCT04189172
SponsorAesculap AG
Last Modified on16 June 2022


Yes No Not Sure

Inclusion Criteria

Written informed consent
Age > 18 years
Duraplasty using Neuro-Patch® according to the Instructions for Use

Exclusion Criteria

Use in infected regions
Use in open cerebrocranial traumata
Use in open spina bifida
Known hypersensitivity to implant materials
Representation by a legal guardian or under involuntary commitment
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Primary Contact



Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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