跳至主要内容
临床试验/CTRI/2022/09/045786
CTRI/2022/09/045786招募中不适用

Microbial Evaluation and Knot Safety of Different Suture Materials in Patients Undergoing Endodontic Microsurgery-A Randomized Controlled Trial.

SGT University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年9月26日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Reduction in total bacterial count.

研究概览

简要总结

Once the patient is selected according to the mentioned criteria , patients will be anesthetized, a full thickness flap will be reflected followed by osteotomy. Periapical endodontic surgery will be performed with the aid of an operating microscope followed by flap approximation and suturing of the surgical site. Suture removal will be carried out 3-5 days. On the day of suture removal, all sutures will be assessed under a surgical microscope and a digital camera. Each suture will then be cut and collected using separate sterile forceps and scissors and transferred to the lab and prepared for microbial analysis.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
25.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • 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 roots.
  • 5 Cooperative patients.

排除标准

  • 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 the American Society of Anesthesiologists class III-VI.
  • 5 Uncooperative patients.

结局指标

主要结局

Reduction in total bacterial count.

时间窗: 3to 5 days

次要结局

  • knot safety of different sutures.(3 to 5 days)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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