Comparative evaluation of efficacy of gingival retraction using three different gingival retraction system with aluminium chloride astringent; retraction cord, copper wire reinforced retraction cord and astringent retraction paste: A randomised control study.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Clinically acceptable retraction will be achieved.
研究概览
简要总结
Patients for this study will be selected from O.P.D of department ofprosthodontics, at the Manubhai Patel dental college, Vadodara. Patients will be informed about the nature of then investigation;and written informed consent will be obtained prior to enrolment. After signing the consent form, each subject will undergo a completeoral examination by the principle investigator. Diagnostic impressions of the upperand lower arches will be made and the impressions will be poured in type IVdental stone. After tooth preparation, impression will be made withgingival retraction and impression will be poured in type IV dental stone. The casts that obtained from the die stone,will be sectioned perpendicular to the coronal plane at the center of the prepared tooth with thehelp of a mechanical saw. Thesesectioned casts will be used for measurement under the stereomicroscope.
研究设计
- 研究类型
- Interventional
- 分配方式
- Random Number Table
- 盲法
- Outcome Assessor Blinded
入排标准
- 年龄范围
- 25.00 Year(s) 至 40.00 Year(s)(—)
- 性别
- All
入选标准
- •Clinically healthy gingiva and periodontium around the teeth Properly root canal treated teeth/vital teeth Maxillary/Mandibular 1st molar.
排除标准
- •Tipped, tilted or rotated abutment teeth Patients with gingival recession, high plaque index, bleeding on probing, pernicious oral habits, hormonal imbalance, immunocompromised and debilitating pre-existing systemic conditions.
结局指标
主要结局
Clinically acceptable retraction will be achieved.
时间窗: 2 years
次要结局
- astringent retraction paste will have good gingival bleeding control capacity(2 years)
