DRKS00024587尚未招募未知
Root coverage using subepithelial connective tissue grafts from different layers of the masticatory mucosa at the hard palate: a randomized controlled trial assessing clinical, volumetric, histomorphometric and patient-centered outcomes
Goethe-Universität Frankfurt | Campus Niederrad Zentrum der Zahn-, Mund- und Kieferheilkunde Carolinum Zahnärztliches Universitäts-Institut gGmbH0 个研究点目标入组 14 人开始时间: 2021年2月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 14
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •Male and female, systemically healthy patients, at least 18 years of age, presenting six adjacent buccal gingival recession defects in the lower jaw (at least one of these with a depth = 2mm) requiring surgical intervention.
- •Masticatory mucosa of the palate between canine and first molar has to be 2.5 mm thick
- •Patients should be treatment naïve with regard to root coverage procedures. Pre-treatment should include therapy of gingivitis, if necessary, instructions in non-traumatic oral hygiene and reconstruction of the cemento-enamel junction with adhesive dental restorations in case of cervical abrasion, erosion, caries or in case of pre-existing insufficient cervical fillings.
- •Periodontal health (no active periodontal disease) including the ability to achieve good oral hygiene and control gingivitis with full-mouth plaque score (FMPS) and full-mouth bleeding score (FMBS) = 25%.
- •No medication known to interfere with periodontal tissue health or healing.
- •No contraindication for elective periodontal plastic surgery.
- •Non-smokers.
- •No pregnancy.
- •Ability to understand study procedures and to comply with them for the entire duration of the study. Ability and willingness to give written informed consent.
排除标准
- •Persistence of uncorrected gingival trauma from tooth brushing.
- •Interdental attachment loss greater than 1mm.
- •Presence of severe tooth malpositioning, rotation or extrusion.
- •Presence of any kind of indirect dental restoration involving the buccal structures of the cemento-enamel junction.
- •Presence of active caries lesions or any evidence of acute or chronic pulpal pathology involving the surrounding periodontal tissues.
- •Participation in another clinical trial, inability or unwillingness to give written informed consent or any other non-fulfilment of any of the above-mentioned inclusion criteria.
研究者
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