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

This study has been completed.

Sponsor:

Information provided by:

University Hospital Freiburg

ClinicalTrials.gov Identifier:

NCT00946049

First received: July 22, 2009

Last updated: July 23, 2009

Last verified: July 2009

History of Changes

Tracking Information
First Received Date ^ICMJE	July 22, 2009
Last Updated Date	July 23, 2009
Start Date ^ICMJE	March 2005
Primary Completion Date	June 2007 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	Complete list of historical versions of study NCT00946049 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Oral Bacteria on Suture Materials - Clinical Comparison of an Antibacterial-coated and a Non-coated Suture Material
Official Title ^ICMJE	Oral Bacteria on Suture Materials - Clinical Comparison of an Antibacterial-coated and a Non-coated Suture Material (VICRYL PLUS® vs. VICRYL®, Ethicon) in Intraoral Dentoalveolar Surgery
Brief 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.
Detailed Description	Not Provided
Study Type ^ICMJE	Interventional
Study Phase	Not Provided
Study Design ^ICMJE	Primary Purpose: Treatment
Condition ^ICMJE	Bacterial Colonization
Intervention ^ICMJE	Device: Vicryl Plus Device: Vicryl
Study Arm (s)	Experimental: Vicryl Plus Intervention: Device: Vicryl Plus Active Comparator: Vicryl Intervention: Device: Vicryl
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Enrollment ^ICMJE	Not Provided
Completion Date	February 2008
Primary Completion Date	June 2007 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	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: 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
Gender	Both
Ages	18 Years to 50 Years
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Germany

Administrative Information
NCT Number ^ICMJE	NCT00946049
Other Study ID Numbers ^ICMJE	323/05
Has Data Monitoring Committee	No
Responsible Party	Not Provided
Study Sponsor ^ICMJE	University Hospital Freiburg
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	University Hospital Freiburg
Verification Date	July 2009
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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