CTRI/2022/09/045539已完成4 期
A Randomized Controlled Trial of Postoperative Pain Evaluation Subsequent to Working Length Determination With And Without Integrated Apex Locator Endomotor While Using A Single File Rotary System In Endodontic Patients
All India Institute Of Medical Sciences Jodhpur0 个研究点目标入组 120 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Healthy patients without systemic diseases or allergic reactions (ASA I and ASA II).
- •2.Mature mandibular first or second molar teeth with symptomatic apical periodontitis and symptomatic irreversible pulpitis.
- •3.Visual analogue scale (VAS) value of either preoperative pain or pain on percussion higher than 50.
- •4.No associated mobility of the tooth
- •5.Patients falling in the age group 14-65 years
- •6.Patients giving verbal and written consent to be included in the study.
排除标准
- •1.Patients with systemic diseases, swelling, sinus tract, preoperative palpation pain.
- •2.Patients with bruxism or clenching.
- •3.Severely damaged tooth.
- •4.Patients who have taken analgesics during past 24 hours.
- •5.Absence of opposing tooth to the related tooth.
- •6. Patients reporting with history of previous endodontic treatment.
- •7. Radiographic evidence of resorption (internal/external), root fracture, calcification,
- •advanced bony destruction.
- •8.Those who will deny consent to participate in the study.
研究者
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