跳至主要内容
临床试验/CTRI/2023/06/054239
CTRI/2023/06/054239尚未招募2 期

Efficacy of a minimally invasive buccal roll technique for peri-implant soft tissue augmentation in the mandibular posterior region - A randomized controlled trial - NI

Dr Shiphalika Sinha0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • No systemic diseases or pregnancy.
  • No probing depths >= 5mm.
  • Full-mouth plaque score (FMPS) and full mouth bleeding score (FMBS) <= 15%
  • (measured at four sites per tooth).
  • Need of soft tissue augmentation in
  • mandibular posterior sites to maintain the
  • natural ridge contour and increase the
  • thickness of tissue buccolingually.
  • No previous soft tissue augmentation
  • procedure at experimental site.

排除标准

  • Disease affecting connective tissue
  • Pregnant or lactating women
  • Untreated periodontal disease.
  • Dental implants previously uncovered or
  • applied with a single -stage procedure.
  • No residual keratinized tissue (KT) at
  • experimental area.
  • Radiographs revealing presence of bone on
  • the cover screw.

研究者

发起方
Dr Shiphalika Sinha

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