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The objective of the study is to clinically assess the safety and effectiveness of LIQOSEAL® as a means of reducing intra- as well as post-operative CSF leakage in patients undergoing elective cranial intradural surgery with a dural closure procedure to show noninferiority compared to a control group.
Enrollment
Sex
Ages
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Inclusion criteria
pre-operative
intra-operative
Exclusion criteria
pre-operative
intra-operative
Primary purpose
Allocation
Interventional model
Masking
228 participants in 2 patient groups
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Central trial contact
Andrew Carlson
Data sourced from clinicaltrials.gov
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