CTRI/2017/02/007774已完成4 期
EVALUATION OF POST OPERATIVE PAIN IN SINGLE VISIT ROOT CANAL TREATMENT WITH PROTAPER NEXT AND M TWO ROTARY SYSTEMS IN ASYMPTOMATIC IRREVERSIBLE PULPITIS OF MULTIROOTED TEETH-A RANDOMIZED CLINICAL TRIAL.
Narayana dental college and hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年2月22日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- post treatment pain evalution using visual analog scale after 8hours,12 hours,24hours,48hours,72hours
研究概览
简要总结
This study is randomised clinical trail to evaluate the post operative pain in single visit root canal treatment by using two different rotary instruments, that will be conducted in narayana dental college and hospital. the primary outcome measureswill be visual analog scale after 8, 24, 48, 72 hours
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Multi rooted teeth with asymptomatic irreversible pulpitis with normal periapical radiographic appearance and periapical radiolucency less than 2mm will be scheduled for initial endodontic treatment.
- •2.Patients of age group between 18-50 3.Subjects who will show prolonged response even after the removal of the stimulus.
- •Patient who has the ability to understand the use of pain scales will be provided informed consent for endodontic treatment.
排除标准
- •1.Patients with sinus tract, periapical abscess or facial cellulitis.
- •2.Patient with known allergies, or any contraindication to opioid or non-opioid analgesics including aspirin or NSAIDs. Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine.
- •Presence of systemic diseases like cardiovascular disease, renal disease, and any bleeding disorders or anti coagulant use with in last month.
- •3.Pregnants and lactating mothers.
- •4.Patients under pain medication for any other illness.
- •Patients who are unable or unwilling to complete the pain questionnaires;
- •Patients who are unwilling to sign consent for endodontic treatment.
结局指标
主要结局
post treatment pain evalution using visual analog scale after 8hours,12 hours,24hours,48hours,72hours
时间窗: post treatment pain evalution using visual analog scale 8hours,12 hours,24hours,48hours,72hours
次要结局
- post treatment pain evalution using visual analog scale(pain evaluation 24, 48, 72 hours after treatment)
研究者
研究点 (1)
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