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临床试验/CTRI/2019/07/019960
CTRI/2019/07/019960尚未招募不适用

Effect of three different methods of working length determination during root canal preparation on post operative pain - An in vivo study

Department of conservative dentistry and endodontics1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年1月7日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Post operative pain

研究概览

简要总结

Theaim of the present study will be to clinically evaluate the post operative painduring root canal preparation , with three different methods of working lengthpreparation.

Suitable number ofpatients will be selected for this in-vivo study . Single rooted tooth will betaken into consideration for this study . Healthy young patients havingirrerversible pulpitis with  toothpositive to a percussion test , negative to palpation test  and without any periapical lesion or any systemicdisease will be included in this study

Patients which will beexcluded from the study according to the following criteria: those withsystemic diseases, swelling, sinus tract, or preoperative palpation pain , thosehaving bruxism or clenching , a severely damaged tooth, severe periodontaldisease in related tooth or resorption in related tooth , having previouslyundergone root canal treatment in related tooth.

A digital radiograph willbe used to confirm the presence of single root for the tooth to be operated on. Preoperative pulpal diagnosis will be performed by both cold test andElectric pulp test .Periapical diagnosis will be performed by periapical radiographsand percussion and palpation tests  .

Patients will be randomlydistributed into 3 experimental groups viz. Radiographic group, Electronic apex locator group and Simultaneous Prepared Group; with equal number of  patients  in each group. After the root canal preparations , patient will be evaluated for postoperative pain after 24hrs ,48 hrs & 72 hrs respectively , keeping in mindno anaelgesics were given post-operatively before pain evaluation . Patientwill respond for pain after percussion on a designed visual analogue scale forpain.

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
12.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Acute pain in single rooted tooth.

排除标准

  • Patient with systemic disease ,sinus tract , periapical lesion ,swelling and sinus tract , bruxism , severely damaged tooth and severe periodontal disease.

结局指标

主要结局

Post operative pain

时间窗: pain evaluation at 24 hours, 48 hours and 72 hours

次要结局

  • Patients will be evaluated for need of post operative analgesics(24 Hours)

研究者

发起方
Department of conservative dentistry and endodontics
申办方类型
Government medical college

研究点 (1)

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