Efficacy of Antimicrobial Coating Suture Coated Vicryl Plus Compared With Vicryl in Reduced Surgical Site Infection of Dental Implant Surgeries: A Uni-Blind Randomized Clinical Trial Study
- Conditions
- Infection, Surgical Site
- Interventions
- Drug: Vicryl plus
- Registration Number
- NCT03659344
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Patients randomly aligned in 2 groups.Vicryl plus sutures were used in group 1 for closing subperiostal flaps after dental implant surgeries and vicryl sutures were used in group 2.
- Detailed Description
Patients were divided randomly based on computer randomization list in two groups: In group1, vicryl plus 4-0 (Vicryl Plus Ethicon,Johnson \& Johnson Company, Sommerville, NJ) suture was used to close surgical site and Vicryl 4-0 (Vicryl Ethicon,Johnson \& Johnson Company, Sommerville, NJ) in group II.
All dental implants were placed through creating subperiosteal flaps. In each group, fresh socket placed dental implants were documented. Patients were visited in 1, 2, 3 and 4 weeks after dental implant surgeries.
Postoperative infection was defined as local erythematous change in the sutured wound with purulent discharge or localized abscess formation on surgical site. If wound dehiscence occurred, it was documented.
Patients were blind about what suture was used.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 320
- Need 3 dental implants at the posterior of the mandible
- Diabetic patients
- smoker
- poor oral hygiene
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Vicryl plus Vicryl plus In this group, vicryl plus(Triclosan coated) sutures were used to close flaps
- Primary Outcome Measures
Name Time Method The prevalence of post-operative infection In one month The number of participants who had local erythematous change in the sutured wound with purulent discharge or localized abscess formation on surgical site.
The prevalence of post-operative dehiscence In one month The number of participants who had relatively or completely open wound
- Secondary Outcome Measures
Name Time Method