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NCT03812120

L-PRF in Cranial Surgery

Status unknown NA Last updated 22 January 2019
What this trial tests

NA trial testing Dural closure with L-PRF in Cranial Sutures; Closure in 350 participants. Status unknown.

Timeline
1 December 2018
Primary endpoint
31 December 2022
31 December 2023

Quick facts

Lead sponsorUniversitaire Ziekenhuizen KU Leuven
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment350
Start date1 December 2018
Primary completion31 December 2022
Estimated completion31 December 2023
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Universitaire Ziekenhuizen KU Leuven — full company profile →

Who can join

18 and older, any sex, with Cranial Sutures; Closure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Leukocyte- and platelet-rich fibrin in cranial surgery: a single-blinded, prospective, randomized controlled noninferiority trial.
    Coucke B, De Vleeschouwer S, van Loon J, Van Calenbergh F, et al · · 2024 · cited 3× · PMID 38394657 · DOI 10.3171/2023.12.jns232125
  2. Leukocyte- and platelet-rich fibrin in cranial surgery: study protocol for a prospective, parallel-group, single-blinded randomized controlled non-inferiority trial {1}.
    Coucke B, Van Hoylandt A, van Loon J, Van Calenbergh F, et al · · 2023 · cited 1× · PMID 36959672 · DOI 10.1186/s13063-023-07252-w

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