Evaluation of Postoperative Pain After Partial Pulpotomy Versus Full Root Canal Treatment in Managing Young Permanent Molars With Symptomatic Irreversible Pulpitis: a Randomized Controlled Trial
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Post operative pain
研究概览
简要总结
The goal of this clinical trial is to assess post-operative pain of partial pulpotomy using a newly introduced Bioceramic material in young patients with symptomatic irreversible pulpitis at 24, 48, 72 hours postoperatively using visual analogue scale (VAS). The main question[s] it aims to answer are:
• In patients with symptomatic irreversible pulpitis does the use of bioceramic material in partial pulpotomy decrease amount of post operative pain in comparison to conventional root canal treatment?
Participants will record the intensity of pain at 24,48, 72 hours postoperatively.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 9 Years 至 14 Years（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •Teeth with acute dentoalveolar abscess.
- •Subjects having more than one tooth that require root canal treatment.
- •Subjects that have taken analgesic, anti-inflammatory or antibiotic drugs during the 10 days prior to the start of treatment.
- •Subjects with systemic diseases who have endocrine diseases, Infectious diseases or Psychological disturbance.
- •Teeth with periodontal disease or pulp calcification.
- •Subjects taking chronic pain medications.
结局指标
主要结局
Post operative pain
时间窗: After 72 hours
Measure intensity of post operative pain using visual analogue scale (VAS)
次要结局
未报告次要终点
研究者
Mohamed Omaia Ahmed Salah
Lecturer of Endodontics
October 6 University