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Clinical trial

A Randomised Controlled Study to Evaluate the Efficacy and Safety of Fibrin Sealant, Vapour Heated, Solvent/Detergent Treated FS VH S/D 500 S-apr (Tisseel) Compared to DuraSeal Dural Sealant as an Adjunct to Sutured Dural Repair in Cranial Surgery.

NCT02891070 is registered in ClinicalTrials.gov with Baxter Healthcare Corporation as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomised Controlled Study to Evaluate the Efficacy and Safety of Fibrin Sealant, Vapour Heated, Solvent/Detergent Treated FS VH S/D 500 S-apr (Tisseel) Compared to DuraSeal Dural Sealant as an Adjunct to Sutured Dural Repair in Cranial Surgery.
Lead sponsor
Baxter Healthcare Corporation
Phase
Phase 3
Overall status
Completed
Start date
October 11, 2016
Completion date
August 22, 2018
Enrollment
224 (actual)
Sites
25

Conditions

As the registry lists them; a condition with its own page is linked.