Evaluation of Socket Shield Technique With Immediate Implant Placement in the Esthetic Zone
2022年6月4日 更新者:Egyptian Russian University
The study was conducted on 20 immediate implant placement sites in the anterior maxillary region.
In the study group, 10 implants were inserted using socket shield technique, while in control group, 10 implants were inserted using conventional immediate placement technique.
All patients received immediate and 6 months post-operative CBCT to assess horizontal bone loss, vertical bone loss, and measurement of bone density.
Implant stability quotients (ISQs) was measured immediately, 1st, 3rd and 6 months post-operatively.
研究概览
详细说明
Unrestorable tooth extraction with immediate implant placement is considered one of the best treatment options in restoring the esthetics and function.
Extraction socket resorption is considered a challenging procedure when it involves the esthetics zone.
The preservation of the entire attachment apparatus for complete preservation of the alveolar ridge makes socket shield technique a promising procedure that helps to maintain anatomy, esthetics and function.
Socket shield technique, eliminate the negative consequences of bone resorption of the buccal plate of bone; leading to maintaining hard and soft tissue contours and provides a perfect pleasing esthetic result with good function.
It is a highly promising technique in terms of maintaining pink and white esthetics through preservation of the interdental papilla during preparation of the interdental socket shield.
It is considered a minimally invasive surgical procedure and offers the advantages of immediate implant placement.
研究类型
介入性
注册 (实际的)
20
阶段
- 不适用
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
-
-
-
Ismailia、埃及
- Suez Canal University
-
-
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
21年 至 65年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Endodontic or non-endodontic treated un-restorable remaining root/ tooth related to maxillary anterior teeth.
- Healthy adult patients > 20 years old (ASAI, II) .
- Adequate oral hygiene.
- Intact periodontal tissues.
Exclusion Criteria:
- Periapical or periodontal active infection involving the teeth/root to be extracted (as excluded by radiographic examination).
- Medically compromised patients (ASA III, IV, V).
- Patients receiving chemotherapy or radiotherapy.
- Heavy smokers,alcohol or drug abuse.
- Patients with parafunctional habits such as bruxism, clenching, excessive gum chewing, lip or fingernail biting.
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:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Study group: implants were inserted using socket shield technique at the esthetic zone
|
Evaluation of socket shield technique with immediate implant placement at the esthetic zone in comparison with the conventional immediate implant placement
|
|
无干预:Control group: implants were inserted using conventional immediate technique
|
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 |
|---|---|---|
|
Implant stability
大体时间:immediate postoperative
|
Using osstell
|
immediate postoperative
|
|
Implant stability
大体时间:one month post-operative
|
Using osstell
|
one month post-operative
|
|
Implant stability
大体时间:three month post-operative
|
Using osstell
|
three month post-operative
|
|
Implant stability
大体时间:six month post-operative
|
Using osstell
|
six month post-operative
|
|
Horizontal gap
大体时间:immediate postoperative
|
Using cone-beam computed tomography
|
immediate postoperative
|
|
Horizontal gap
大体时间:six month post-operative
|
Using cone-beam computed tomography
|
six month post-operative
|
|
Vertical bone loss
大体时间:immediate postoperative
|
Using cone-beam computed tomography
|
immediate postoperative
|
|
Vertical bone loss
大体时间:six month post-operative
|
Using cone-beam computed tomography
|
six month post-operative
|
|
Bone density
大体时间:immediate postoperative
|
Using cone-beam computed tomography
|
immediate postoperative
|
|
Bone density
大体时间:six month post-operative
|
Using cone-beam computed tomography
|
six month post-operative
|
|
peri-implant probing depth
大体时间:immediate postoperative
|
using periodontal probe
|
immediate postoperative
|
|
peri-implant probing depth
大体时间:one month post-operative
|
using periodontal probe
|
one month post-operative
|
|
peri-implant probing depth
大体时间:three month post-operative
|
using periodontal probe
|
three month post-operative
|
|
peri-implant probing depth
大体时间:six month post-operative
|
using periodontal probe
|
six month post-operative
|
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。
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)
2019年9月16日
初级完成 (实际的)
2021年1月6日
研究完成 (实际的)
2021年9月7日
研究注册日期
首次提交
2022年5月24日
首先提交符合 QC 标准的
2022年6月4日
首次发布 (实际的)
2022年6月8日
研究记录更新
最后更新发布 (实际的)
2022年6月8日
上次提交的符合 QC 标准的更新
2022年6月4日
最后验证
2022年6月1日
更多信息
与本研究相关的术语
其他研究编号
- HR-1
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不
研究美国 FDA 监管的设备产品
不
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