Connective Tissue Grafting for Single Tooth Recession & the Impact of the Thickness of the Palatal Harvest Tissue
2017年1月24日 更新者:Evanthia Lalla、Columbia University
Connective Tissue Grafting for Single Tooth Recession Defects & the Impact of the Thickness of the Palatal Harvest Tissue: A Pilot Study
The purpose of this study is to test if the thickness of the graft taken from the roof of the mouth, has a significant effect on the amount of attached tissue and the amount of root coverage that are attained when treating a single tooth with gingival recession.
研究概览
详细说明
The goal of the study is to determine if the thickness of a tissue graft taken from the roof of the mouth, used to cover the exposed root of a tooth, affects the overall outcome of the root coverage, the health of the resulting tissue, as well as postoperative pain as reported by the patient.
Connective tissue grafts will be harvested in different thicknesses, and results of the procedures will be compared.
Qualified subjects will undergo a root coverage procedure, after random assignment to one of the groups.
Regular recall visits to monitor healing at intervals of 1 week, 2 weeks, 1 month, and 3 months will be scheduled.
Subjects will be asked to fill out patient response forms regarding pain and other symptoms at these visits.
Photographs will be taken.
研究类型
介入性
注册 (实际的)
42
阶段
- 不适用
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
18年 及以上 (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:
- Age>18 years old
- Absence of active periodontal disease
- Single tooth (premolars and anterior teeth) with Miller class I or II gingival recession >= 2mm
- Detectable Cemento-Enamel Junction (CEJ) -
Exclusion Criteria:
- Smokers (>10 cigarettes/ per day)
- Uncontrolled systemic diseases with compromised healing potential (DM with HbA1c >7%)
- Active infectious diseases (hepatitis, tuberculosis, HIV, etc.)
- Medication known to cause gingival enlargement
- Patients taking anticoagulants with an international normalized ratio (INR) >2.5
- Long-term (>2 weeks) use of antibiotics in the past 3 months
- Pregnant or attempting to get pregnant
- Sites with probing depth > 4mm
- Recession adjacent to an edentulous area
Frenal and muscle attachment that encroach on the marginal gingiva
a. Can be included 2 months after surgical therapy to remove the frenum (frenectomy)
- History of periodontal surgical treatment of the involved sites
- Prosthetic crown, restorations or caries in the candidate tooth and adjacent teeth
- Teeth with pulpal pathology
- Severe teeth malposition and open contacts
- Planned orthodontic treatment to commence within 1 year following procedure
- Parafunctional habits -
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:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
---|---|
有源比较器:1mm thick graft
connective tissue graft of 1mm thickness
|
palatal connective tissue graft to attain root coverage
|
有源比较器:2mm thick graft
connective tissue graft of 2mm thickness
|
palatal connective tissue graft to attain root coverage
|
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 |
---|---|---|
Root coverage
大体时间:Upto 3 months
|
Amount of root coverage attained in millimeters
|
Upto 3 months
|
Root coverage
大体时间:Upto 3 months
|
Amount of root coverage attained in percentage
|
Upto 3 months
|
width of keratinized tissue
大体时间:Upto 3 months
|
Amount of zone of keratinized tissue attained in millimeters
|
Upto 3 months
|
width of keratinized tissue
大体时间:Upto 3 months
|
Amount of zone of keratinized tissue attained in percentage
|
Upto 3 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
---|---|---|
thickness of keratinized tissue
大体时间:Upto 3 months
|
Upto 3 months
|
|
amount of erythema and edema
大体时间:Upto 3 months
|
patient reported outcome of amount of erythema and edema in number of days postoperatively
|
Upto 3 months
|
duration of erythema and edema
大体时间:Upto 3 months
|
patient reported outcome of duration of erythema and edema in number of days postoperatively
|
Upto 3 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:Evanthia Lalla, DDS、Columbia 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
2014年10月1日
初级完成 (实际的)
2016年5月1日
研究完成 (实际的)
2016年5月1日
研究注册日期
首次提交
2017年1月11日
首先提交符合 QC 标准的
2017年1月24日
首次发布 (估计)
2017年1月26日
研究记录更新
最后更新发布 (估计)
2017年1月26日
上次提交的符合 QC 标准的更新
2017年1月24日
最后验证
2017年1月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
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