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NCT03883022

Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery

Recruiting now NA Last updated 20 March 2019
What this trial tests

NA trial testing with U-VANCO (vancomycin hydrochloride) in Spinal Fusion in 400 participants. Currently enrolling.

Timeline
3 September 2018
Primary endpoint
12 September 2027
31 December 2027

Quick facts

Lead sponsorTaipei Veterans General Hospital, Taiwan
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment400
Start date3 September 2018
Primary completion12 September 2027
Estimated completion31 December 2027
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Taipei Veterans General Hospital, Taiwan

Who can join

20 and older, any sex, with Spinal Fusion or Spinal Stenosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Deep surgical site infection (DSSI) is one of the most challenging complications for spinal surgeons and can lead to a poor clinical outcome. This ambispective study was designed to examine the effect of vancomycin powder mixed with autogenous bone graft and bone substitute on preventing deep surgical site infection (DSSI) in degenerative lumbar fusion surgeries as well as any interference with bony fusion.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Vancomycin powder mixed with autogenous bone graft and bone substitute may decrease the deep surgical site infections in elective lumbar instrumented fusion surgery for degenerative disorders: a prospective randomized study.
    Wang ST, Lin HH, Yao YC, Huang N, et al · · 2025 · cited 1× · PMID 40334989 · DOI 10.1016/j.spinee.2025.05.001

Verify or expand the search:

Other recruiting trials for Spinal Fusion

Currently open trials in the same condition.

Other Taipei Veterans General Hospital, Taiwan trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03883022.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing