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Study identifier: NCT07386366 Synced from ClinicalTrials.gov · July 29, 2026
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Wound Healing and Bacterial Adherence With Triclosan-Coated Sutures After Mandibular Impacted Third Molar Surgery

Condition: Impacted Mandibular Third Molar · Postoperative Wound Healing  ·  Sponsor: University of Medicine and Pharmacy at Ho Chi Minh City

PhaseNA
Planned participants14
Who can joinAll sexes, 18 Years to 35 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to learn if triclosan-coated absorbable stitches (polyglactin 910 sutures coated with triclosan, an antibacterial agent) help soft tissue heal better and have fewer bacteria stuck to the stitches after lower impacted wisdom tooth surgery in adults aged 18 to 35 years. The main questions it aims to answer are: 1. Does triclosan-coated polyglactin 910 suture lead to better soft-tissue wound healing than non-coated polyglactin 910 suture on postoperative days 3, 5, and 7 after mandibular impacted third molar surgery? 2. Does triclosan-coated polyglactin 910 suture result in a lower oral bacterial load adhered to the suture material than non-coated polyglactin 910 suture on postoperative days 3, 5, and 7 after mandibular impacted third molar surgery? Participants will: * Have surgery to remove two similar lower impacted wisdom teeth (one on each side) * Receive triclosan-coated stitches on one side and standard stitches on the other side, with the side assignment chosen at random * Return for follow-up visits on day three, day five, and day seven after surgery for healing checks, simple ratings of pain and swelling, and collection of a small stitch sample for bacterial testing.

This description comes directly from the study's public registry record.

Talk to the study team

Le Khanh Huyen Nguyen  ·  84981869502  ·  nlkhuyen.ths.rhm24@ump.edu.vn

Always discuss trial participation with your own doctor first.

Locations (1)

Specialized Dental Clinic, University of Medicine and Pharmacy at Ho Chi Minh CityHo Chi Minh City, VietnamRecruiting

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Source record: clinicaltrials.gov/study/NCT07386366