UnknownNot Applicable

L-PRF in Cranial Surgery

Belgium350 participantsStarted 2018-12-01

Plain-language summary

The investigators want to demonstrate in a prospective, randomized trial including 350 patients undergoing cranial surgery that the use of L-PRF is non-inferior to classical fibrin sealants.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients undergoing cranial neurosurgery whereby the dura is intentionally opened (supratentorial and infratentorial approach) * Age ≥ 18 years * Written informed consent * Willing to comply with the study schedule Exclusion Criteria: * Participation in another clinical trial with study drugs or devices * Pregnancy

What they're measuring

Success rate

Timeframe: 4 years

Trial details

NCT IDNCT03812120

SponsorUniversitaire Ziekenhuizen KU Leuven

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-31

Contact for this trial

Tom Theys, Prof

003216344290 tom.theys@uzleuven.be

View on ClinicalTrials.gov More Cranial Sutures; Closure trials