Evaluation of bacteria and Knot Security of on Different Suture Materials in Patients Undergoing Endodontic surgery-A Randomized Controlled Trial
- Registration Number
- CTRI/2020/02/023405
- Lead Sponsor
- Dr simran verma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
1.Patients Age 25 -45 years consenting to the surgical procedure.
2.Non-contributory medical history (American Society of Anaesthesiologists class I and class II).
3.Endodontic lesions not responding to conventional root canal treatments.
4.Lesion involving not more than 1-3 root
5.Cooperative patients.
1.In patients where tooth is un-restorable, inadequate root length and poor periodontal support.
2.Non consenting patients and patients younger than 25 years of age.
3.Patients with limited mouth opening.
4.Medical history with American Society of Anaesthesiologists class III-VI.
5.Uncooperative patients.
6.Patients with poor oral hygiene.
7.Vertical root fracture.
8.Through and through defects.
9.Close proximity to anatomical structures.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To evaluate and compare microbial colonization on four different suture materials following endodontic microsurgery. <br/ ><br>2.To microscopically assess and compare knot safety of four different suture materials following endodontic microsurgery <br/ ><br>Timepoint: suture removal after 3-5 days post endodontic microsurgery
- Secondary Outcome Measures
Name Time Method 1.To evaluate and compare microbial colonization on four different suture materials following endodontic microsurgery. <br/ ><br>2.To microscopically assess and compare knot safety of four different suture materials following endodontic microsurgery <br/ ><br>Timepoint: sutures will be assessed on the 1st,2nd,3rd,4th,5th day post operatively and removed 3-5 days after the surgery