跳至主要内容
临床试验/DRKS00024587
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

发起方
Goethe-Universität Frankfurt | Campus Niederrad Zentrum der Zahn-, Mund- und Kieferheilkunde Carolinum Zahnärztliches Universitäts-Institut gGmbH

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