Indirect Pulp Treatment in Primary Molars (RCT)
2019年8月28日 更新者:Mohamed Farouk Rashed、Cairo University
Evaluation of Resin Modified Glass Ionomer Liner (Vitrebond™) Versus Calcium Hydroxide as Indirect Pulp Treatment Material Used in Deep Carious Lesions in Primary Molars: A Randomized Clinical Trial
This study was conducted to evaluate the clinical and the radiographic success of Dycal and Vitrebond as indirect pulp treatment materials in primary molars.
研究概览
地位
完全的
条件
详细说明
Evaluation of calcium hydroxide and resin modified glass ionomer liner clinically and radiographically as indirect pulp treatment materials in deep caries in primary molars.
研究类型
介入性
注册 (实际的)
88
阶段
- 第四阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
-
Cairo、埃及、11553
- Faculty of Oral and Dental Medicine
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
4年 至 8年 (孩子)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion criteria:
In compliance with AAPD, 2017 guidelines for pulp therapy "IPT is indicated in a primary tooth with no pulpitis or with reversible pulpitis when the deepest carious dentin is not removed to avoid a pulp exposure. The pulp is judged by clinical and radiographic criteria to be vital and able to heal from the carious insult"
In addition to:
I-Subjects:
- Medically free children, their parent(s) accepts to sign the informed consent.
- Age range from 4-8 years.
II-Molars:
- Presence of at least 1 primary molar with deep carious lesion extending to more than one half of the dentin on radiographic examination (to make the trial regardless of number of carious molars).
- Clinically: Normal mobility and normal appearance of gingiva (vital teeth).
- Radiographically: Normal roots without physiological resorption, normal lamina dura and normal periodontal membrane space (indicated for IPT).
Exclusion criteria:
I-Subjects:
- Uncooperative children.
- Parents unable to attend follow up visits (even after explaining the importance of recall visits).
II-Molars:
- History of spontaneous pain (to exclude reversible pulpitis).
- Clinically: Presence of swelling, sinus, fistula or tooth mobility (to exclude non vital teeth).
- Radiographically: Presence of radiolucent lesions at furcation or periapical region or external or internal resorption (to exclude teeth not indicated for IPT).
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:IPT using Dycal (TM )
Indirect pulp treatment; IPT using Dycal (TM ); (2 paste system) by partial caries removal
|
Partial caries removal and protection of the dental pulp with biocompatible material
其他名称:
Partial caries removal and protection of the dental pulp with biocompatible material
其他名称:
|
|
实验性的:IPT using Vitrebond (TM )
Indirect pulp treatment; IPT using Vitrebond (TM );(powder and liquid) by partial caries removal
|
Partial caries removal and protection of the dental pulp with biocompatible material
其他名称:
Partial caries removal and protection of the dental pulp with biocompatible material
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of cases reporting postoperative pain
大体时间:12 months
|
Presence of postoperative pain following dental treatment through patient questionnaire as a sign of clinical failure
|
12 months
|
|
Number of cases reporting swelling
大体时间:12 months
|
Presence of postoperative swelling following dental treatment through visual examination using hand mirror as a sign of clinical failure
|
12 months
|
|
Number of cases reporting sinus
大体时间:12 months
|
Presence of sinus following dental treatment through visual examination using hand mirror as a sign of clinical failure
|
12 months
|
|
Number of cases reporting fistula
大体时间:12 months
|
Presence of fistula following dental treatment through visual examination using hand mirror as a sign of clinical failure
|
12 months
|
|
Number of cases reporting tooth mobility
大体时间:12 months
|
Presence of abnormal tooth mobility following dental treatment through tactile examination using two hand mirrors as a sign of clinical failure
|
12 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of cases reporting external root resorption
大体时间:12 months
|
Occurrence of pathological external root resorption following dental treatment through parallel periapical radiographic examination as a sign of radiographic failure
|
12 months
|
|
Number of cases reporting internal root resorption
大体时间:12 months
|
Occurrence of pathological internal root resorption following dental treatment through parallel periapical radiographic examination as a sign of radiographic failure
|
12 months
|
|
Number of cases reporting furcation involvement
大体时间:12 months
|
Occurrence of pathological internal root resorption following dental treatment through parallel periapical radiographic examination as a sign of radiographic failure
|
12 months
|
|
Number of cases reporting widening of periodontal membrane space
大体时间:12 months
|
Occurrence of widening of periodontal membrane space following dental treatment through parallel periapical radiographic examination as a sign of radiographic failure
|
12 months
|
|
Number of cases reporting periapical radiolucency
大体时间:12 months
|
Occurrence of periapical radiolucency following dental treatment through parallel periapical radiographic examination as a sign of radiographic failure
|
12 months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Shereen E Taha, Professor、Cairo University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2016年8月1日
初级完成 (实际的)
2017年8月1日
研究完成 (实际的)
2018年7月1日
研究注册日期
首次提交
2018年8月18日
首先提交符合 QC 标准的
2018年12月7日
首次发布 (实际的)
2018年12月10日
研究记录更新
最后更新发布 (实际的)
2019年8月30日
上次提交的符合 QC 标准的更新
2019年8月28日
最后验证
2019年8月1日
更多信息
与本研究相关的术语
其他研究编号
- CEBD-CU-2014-11-3
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
IPD 计划说明
final results
药物和器械信息、研究文件
研究美国 FDA 监管的药品
是的
研究美国 FDA 监管的设备产品
不
在美国制造并从美国出口的产品
是的
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