Comparative Clinical and Radiographic evaluation of Zinc oxide Ozonated Olive Oil as Obturation material in Primary molars with different Obturation techniques: An In vivo Study
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
研究概览
简要总结
This study is a randomized, double-blind, parallel-group in vivo clinical trial evaluating zinc oxide mixed with ozonated olive oil as an obturation material in primary mandibular molars of children aged 4–8 years. A total of 40 children requiring pulpectomy will be included and randomly allocated into two groups, 20 in each. The intervention group will receive obturation using the Navitip syringe technique to deliver the zinc oxide–ozonated olive oil mixture into the prepared canals. The comparator group will receive obturation using the Lentulo spiral technique with the same obturating material. The primary outcome includes evaluation of the quality of obturation in terms of fil that includes optimal fil, underfil, or overfil)and presence of voids. Secondary outcomes will include clinical and radiographic evaluation of obturation quality based on length of filling and the presence of voids during follow-up.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 4.00 Year(s) 至 8.00 Year(s)(—)
- 性别
- All
入选标准
- •Healthy cooperative children aged 4-8 years 2.Mandibular primary molars with irreversible pulpitis devoid of any other diseased teeth in that quadrant that bothers the patient 3.No history of analgesic use 12 hours prior to pulpectomy.
排除标准
- •Uncooperative children 2.Children with systemic illness 3.Teeth with clinical and radiographic contraindications for pulpectomy.
研究者
Dr Cherukuri Nikitha Saranya
GITAM Dental College and Hospital
