IRCT2013110215236N1已完成早期 1 期
Treatment of periodontitis and chronic periodontitis and the complications
aser Department, Dental School of Tehran University of Medical Sciences0 个研究点目标入组 44 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 44
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
- 年龄范围
- 35 years 至 60 years（—）
- 性别
- All
入选标准
- •This study is a double –blind randomized clinical trial and is done in a full mouth design. Totally 44 patients to be surveyed in this study . The patient have periodontal pocket with 5 mm depth and more it also needs to be mentioned that these patients have Chronic periodontitis that have not answered to phase one and the periodontal pocket is left in them. It must be said that the age rage is 35 and over it more over. These patients criteria is remaining periodontal pocket after doing phase one. More over to these facts:
- •1.The patients must be without systematic disease.
- •2.Pregnant patients are not to be taken part.
- •3.The patients must not use drugs or smoke.
- •4.The patients must not have used any antibiotic in a 6 month period.
- •The patients go under SRP treatment for the 2nd time after clinical check-up and registering parameters like BOP / CAL / PPD / FMBS / FMPS and PI. If one the 50 patients FMPS is lower than 20% he/she gets radiated in the 1st 2nd and 7th days during 3 sessions in 3 days. In order to se that there is no dental plaque the patients are to be checked-up one week after doing SRP. Every patients left pocket gets radiated with Diode laser and EmunDo. The sensitive substance to light (photosensitizer) The day after check-up in the 1st 3rd and 7th days over a week.
- •In goal group: all teeth go under PDT with Diode laser followed by EmunDo photosensitizer having 300 mw power in 10 seconds and 3 joule energy in 6 adjacent dental points.
- •In beholder group all teeth including those that have periodontal pocket with the depth of 5 mm and more and without periodontal pocket go under SRP with physiologic serum and off laser. than the patients are to be re-studied and compared in one three and six month intervals.
排除标准
- 未提供
研究者
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