L-PRF in Cranial Surgery

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.

Lead sponsor: Universitaire Ziekenhuizen KU Leuven•1 locations•View source on ClinicalTrials.gov

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Contacts

Tom Theys, Prof

CONTACT

003216344290 tom.theys@uzleuven.be

Anais Van Hoylandt, Sc

CONTACT

003216342012 anais.vanhoylands@uzleuven.be

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NCT03910374 · Cranial Sutures; Closure

Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 22, 2019Terms

Trial snapshot

StatusUNKNOWN

PhaseNA

Enrollment350

Start dateDec 2018

Last updatedJan 22, 2019

Condition

Cranial Sutures; Closure

Locations shown

Tom Theys

Leuven

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 22, 2019Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

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