Termoplastik Kor tekniğini Iki farklı Kanal patı Ile kullanıp Tedavi sonrası Hassasiyet ve kök Ucundan taşma miktarının değerlendirilmesi: Randomize kontrollü Klinik çalışma
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 160
- 主要终点
- The incidence of postoperative pain by using VAS scale after obturation with different sealers.
研究概览
简要总结
The aim of this study was to evaluate and compare postoperative pain and overextension of root canal filling after root canal treatment using a carrier-based obturation system and two different sealers.
In this prospective randomized clinical trial, 160 mandibular premolars and molars in 160 patients were treated. Patients with vital and devital teeth were assigned to four groups using a randomized block design with block sizes of 10 patients each. The groups were composed of devital teeth with periapical lesions treated with iRoot SP sealer, vital teeth treated with iRoot SP sealer, devital teeth with periapical lesions treated with AH Plus sealer, and vital teeth treated with AH Plus sealer. In single visits, a single operator prepared root canals and filled them with sealer using the carrier-based obturation technique. Radiographs were taken and obturation length was recorded. Patients recorded pain scores use of Visual Analogue Scale and frequency of analgesic intake at baseline and 0-6, 6-12, 12-24, and 24-72 h..
详细描述
This randomized controlled clinical study was conducted to compare the incidence and intensity of post-obturation pain, evaluate the overextension of filling material radiographically, and assess the relationship between pain and analgesic intake in patients with vital and devital teeth undergoing carrier-based obturation with two different sealers (iRoot SP, AH Plus)
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •no systemic diseases
- •women were not pregnant or breastfeeding status
- •no history of taking analgesics in the previous seven days or other drugs prior to presenting for treatment.
- •all selected teeth were mandibular molar or mandibular premolar.
排除标准
- •systemic and/or periodontal disease;
- •allergy to local anesthetic agents and/or history of intolerance to nonsteroidal anti-inflammatory drugs;
- •requirement for antibiotic prophylaxis
- •open tooth apex
- •pacemaker use
结局指标
主要结局
The incidence of postoperative pain by using VAS scale after obturation with different sealers.
时间窗: 72 hour
次要结局
未报告次要终点
研究者
Ayfer Atav Ateş
Research assistant
Cukurova University