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临床试验/NCT06749158
NCT06749158已完成不适用

Radiographic and Histological Assessment of Guided Bone Regeneration Using Deproteinized Bovine Bone Compared to Spontaneous Bone Regeneration of Maxillary Defects , Resulted From Enucleation of Intra-bony Cystic Lesions : Randomized Control Clinical Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
44
试验地点
1
主要终点
The amount of change in the Bone density

研究概览

简要总结

Two groups of patients with maxillary defects resulted from enucleation of intra-bony cystic lesions the 1st group will be subjected to guided bone regeneration while the second group will be subjected to spontaneous bone regeneration.

详细描述

  • Two groups of patients with maxillary cystic lesions indicated for enucleation. One will be subjected to guided bone regeneration while the other will be subjected to spontaneous bone regeneration.

  • General pre-operative procedures:

  • All patients will undergo appropriate preparation involving periodontal therapy , proper oral hygiene measures in addition to endodontic treatment for the non-vital teeth related to the lesion.

intraoperative procedure: (both groups)

  • Scrubbing and draping of the patient will be carried out in a standard fashion using betadine surgical scrub.
  • Local anesthesia will be administered (Articaine hydrochloride 4% with Epinephrine 1:100,000) injectable solution.
  • Flap design: a sulcular incision will be done , extending two teeth beyond the area of interest followed by two oblique incisions on either side of the flap. A full thickness mucoperiosteal flap will be raised to expose the area occupied by the lesion.
  • After flap reflection, the exposed bone related to the lesion will need to be removed to provide adequate accessibility before enucleation of the lesion.
  • The specimens will be fixed in 10% formalin for pathological examination.

Intra-operative procedures - continued in first Group (GBR group) The intra-bony defect will be filled with Deproteinized Bovine Bone. In Both groups: Titanium mesh will be tailored with 3mm overlap at the edges to cover the bone window completely and fixed to the bone using mono-cortical titanium screws.

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

This trial is considered a randomized single blind clinical trial due to the following:

  • The participants will be blinded to the technique that will be used during the surgical procedure.
  • The operator will not be blinded for both techniques during the surgical procedure as the two techniques are different.
  • The outcome assessor cannot be blinded.

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of a well-defined pathological cystic lesion involving the maxilla, confirmed clinically and radiographically that require surgical enucleation resulting in an intra-bony defect.
  • Mesiodistal dimension of the defect ranging from 1 cm to 4.0 cm.
  • Patients aged 20 to 50 years, of either sex.
  • Patients medically fit for surgical intervention under local or general anesthesia (ASA I or II)
  • Absence of systemic conditions affecting bone healing (e.g., uncontrolled diabetes, osteoporosis)
  • Patients willing to participate in the study and able to provide informed written consent.
  • Availability of adequate postoperative follow-up (minimum of 6 months).

排除标准

  • Pregnant or lactating women.
  • Radiographically, Presence of multi-locular or aggressive lesions suggestive of odontogenic tumors (e.g., ameloblastoma)
  • Patients with compromised immune status (e.g., HIV, long-term corticosteroid therapy)
  • History of allergic reaction to any of the surgical materials used (e.g., titanium, bovine bone graft).
  • Patients participating in another clinical trial or receiving investigational therapy during the study period.
  • Presence of acute infection at the surgical site.
  • cysts with a known high recurrence rate such as Odontogenic keratocysts (OKC).

研究组 & 干预措施

spontaneous bone regeneration

Active Comparator

after cyst enucleation, the intra-bony defect will be covered by Titanium mesh that is fixed by mono-cortical titanium screws.

干预措施: spontaneous bone regeneration (Procedure)

guided bone regeneration

Experimental

cyst enucleation will be followed by filling the intra-bony defect with Deproteinized Bovine Bone.

-Titanium mesh will cover the bone window completely and will be fixed to the bone using mono-cortical titanium screws.

干预措施: guided bone regeneration (Procedure)

结局指标

主要结局

The amount of change in the Bone density

时间窗: 6 months postoperatively

Measuring the amount of change in the bone density using cone beam computed tomography in hounsfield unit

次要结局

  • Percentage of bone area(6 months postoperatively)

研究者

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

Alaa Mohamed Abdelzaher

Principal investigator

Cairo University

研究点 (1)

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