The Comparison of Microbial Adherence to Various Sutures in Patients Undergoing Oral Surgery
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 30
- Primary Endpoint
- bacterial counts on blood agar plates from each suture will be quantified in CFU (colony-forming units) and expressed as total bacteria/suture
Study Overview
Brief Summary
The final stage of any surgical procedure is suturing. Sutures have a vital rule in wound healing- they are responsible for flaps approximation, hemostasis and restoring function and esthetics.
Choosing the right suture is crucial especially in oral sites because of its unique anatomical features: the presence of saliva and the patient's everyday function- swallowing, talking, eating etc.
Sutures require certain physical properties such as tensile strength, dimensional stability, lack of memory, knot security and elasticity. One highly important quality is the ability to prevent or reduce bacterial adhesion and by that to prevent secondary infection. There are many kinds of sutures in the market- none of which contains all the ideal features.
The aim of the study is to compare the amount of bacterial adhesion to different kinds of sutures in patients undergoing periodontal surgery.
Detailed Description
The participates in the study are scheduled to go oral surgery: dental implantation, Guided bone regeneration, resective periodontal surgery, sinus elevation (both crestal or lateral).
All participates will sign an informed consent form and under the institutional ethics committee approval will go to through the operation.
Each surgery will include at least 4 Simple Interrupted Suture with even spacing of 5 mm from each other in the scheduled for operation and without changing the original treatment plan. Incision location is in the area of surgery and not in a distinct location. The four sutures that will be used are: silk, vicryl, nylon and polypropylene.
At suture removal, after 10 days, all sutures will be collected in a sterile tube containing PBS solution. Within 3 hours, the samples will be sowed on two blood agar media plates. One plate will be aerobic condition and the other in an-aerobic condition. After one week, the number of colonies will use to calculate the CFU- colony-forming units.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Patients designated for oral surgery with the possibility to perform at least 4 sutures, 5mm apart. The surgery will take place at the periodontology department, Dental faculty, Hadassah medical center.
- •Patients willing to participate in the study and sign an informed concerned form
- •Patients without systemic illness
Exclusion Criteria
- •Diabetes, heart disease, immune deficiency, thrombocytopenia\ coagulation enzymes deficiency
- •Chronic alcohol consumption\ drug user
- •Pregnancy
Outcomes
Primary Outcomes
bacterial counts on blood agar plates from each suture will be quantified in CFU (colony-forming units) and expressed as total bacteria/suture
Time Frame: Outcome measure will be assessed 10 days after sample incubation for the different sutures obtained from each study participate
CFU from all four different sutures (silk, vicryl, nylon and polypropylene sutures) will be compared.
Secondary Outcomes
No secondary outcomes reported