跳至主要内容
临床试验/NCT03466840
NCT03466840Unknown不适用

Clinical Assessment of Coronally Advanced Lingual Flap to Modified Periosteal Releasing Incision for Flap Advancement in Partially Edentulous Patients Undergoing Guided Bone Regeneration Using Titanium Mesh.

Cairo University2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2018年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
7
试验地点
2
主要终点
Flap advancement

研究概览

简要总结

Comparison of cronally advanced lingual flap to modified periosteal releasing incision (MPRI)

详细描述

Clinical Assessment and Comparison of Coronally Advanced Lingual Flap to Modified Periosteal Releasing Incision for Flap Advancement in Partially Edentulous Patients Undergoing Guided Bone Regeneration Using Titanium Mesh: A Randomized Clinical Trial

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

According to the allocation sequence obtained from the computer software the numbers will be written in small folded opaque papers and put in opaque sealed envelopes. All those papers will be ready before conducting any procedure. The patients will be allowed to pick his/her number from the pile of envelopes and will be assigned accordingly. The number of papers will decrease as each patient picks his number and so on.

入排标准

性别
All
接受健康志愿者

入选标准

  • Partially edentulous patients in the mandibular posterior region.
  • Patients with healthy systemic condition.
  • Insufficient ridge width (< 5mm).
  • Presence of proper inter-arch space for placement of the implant prosthetic part.
  • Adequate soft tissue biotype (≥ 2 mm).

排除标准

  • Patients with systemic conditions that may interfere with the results of the study.
  • Patients with local pathological defects related to the area of interest.
  • Unmotivated, uncooperative patients with poor oral hygiene.
  • Patients with habits that may jeopardize the implant longevity and affect the results of the study such as smoking, alcoholism or para-functional habits.

研究组 & 干预措施

The Coronally Advanced Lingual Flap

Experimental

On the lingual side of mandible, a full-thickness muco-periosteal flap is elevated until reaching mylohyoid line. Using a blunt instrument, a connective tissue band is localized continuing with the epimysium of the mylohyoid muscle and is inserted into the inner part of the lingual flap . The blunt instrument is inserted below the connective band, and with gentle traction in the coronal direction, this muscular insertion was detached from the lingual flap. Using a "periodontal probe" the amount of advancement is measured.

干预措施: The coronally advanced lingual flap (Procedure)

Modified periosteal releasing Incision

Active Comparator

A full-thickness muco-periosteal flap is reflected on the buccal side. Near the base of muco-periosteal flap, the periosteum is incised less than 0.5mm in depth, creating two segments, "coronal segment" and "apical segment," of the periosteal flap. The flap is pulled with a pair of periodontal forceps laterally. Subsequently, the "lateral stretching" of the coronal segment of the flap is performed by applying pressure using the blunt face of scalpel blade, or a blunt instrument, with sweeping motion. This motion helps stretching the flap over the submucosa, thereby permitting the flap to be mobile.Using a "periodontal probe" the amount of advancement is measured

干预措施: Modified periosteal releasing Incision (Procedure)

结局指标

主要结局

Flap advancement

时间窗: "10 minutes"

Flap advancement will be measured as a difference between the value before and after in millimeters using periodontal probe.

次要结局

  • Postoperative Pain(1 Week)
  • Postoperative membrane exposure(12 Weeks)
  • bone density(12 Weeks)
  • postoperative swelling("1 week")

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Noha Fathi Messalam Diab

principal investigator

Cairo University

研究点 (2)

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