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CompletedNCT00946049Updated Jul 24, 2009

Oral Bacteria on Suture Materials - Clinical Comparison of an Antibacterial-coated and a Non-coated Suture Material

An interventional study of Vicryl Plus and Vicryl in Bacterial Colonization, sponsored by University Hospital Freiburg. Completed at 1 site in Germany. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2009-07-24.

Sponsored by University Hospital Freiburg · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Antibacterial Triclosan-coated suture material (VICRYL PLUS®, Ethicon) and non-coated (VICRYL®) was compared for bacterial colonization after third molar extraction. Sutures were removed postoperatively and adhered bacteria were investigated.

02

Conditions studied

  • Bacterial Colonization

Keywords

  • Checking clinical antibacterial effect of Vicryl Plus compared to conventional Vicryl in intraoral surgery
  • Bacteria
03

In context

Lead sponsor

University Hospital Freiburg is the lead sponsor of 91 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • planned surgical extraction of 1 to 4 wisdom teeth
  • no inflammation and pain within the planned surgical area
  • legal age
  • clinically healthy patient

Exclusion criteria

Exclusion Criteria:

  • allergy to Triclosan or phenols
  • gravidity/lactation
  • immunosuppression due to drugs or diseases
  • severe general diseases
  • long-term medication
  • intake or use of other antibiotical drugs/devices
05

Study design

Phase
Not applicable
Primary purpose
Treatment

Study arms

  • Experimental
    Vicryl Plus

    Device: Vicryl Plus

  • Active comparator
    Vicryl

    Device: Vicryl

Interventions

  • DeviceVicryl Plus
  • DeviceVicryl
06

Study locations

1 site
  • Albert-Ludwigs-University Freiburg, Department for Oral and Maxillofacial Surgery
    Freiburg, 79106, Germany
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 24, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00946049
Lead sponsor
University Hospital Freiburg
First posted
Jul 24, 2009
Start date
Mar 2005
Primary completion
Jun 2007
Completion
Feb 2008
Last update
Jul 24, 2009

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2009. You cannot join it, but the record below documents what was studied.

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