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临床试验/NCT07044895
NCT07044895尚未招募不适用

Evaluation of Diode Laser Photocoagulation With Immediate Implant Placement in the Maxillary Esthetic Zone

Hams Hamed Abdelrahman2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2025年6月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
8
试验地点
2
主要终点
Change in wound healing

研究概览

简要总结

Placement of an immediate implant is becoming popular because of its potential in minimizing the treatment time and enhancing the patient comfort and esthetic outcomes. It is crucial to maintain adequate thickness of labial bone with the establishment of a stable and healthy gingival seal around the implant abutment to prevent the invasion of bacteria and peri-implant inflammation. Diode lasers have been developed as a promising tool in dentistry, providing a precise manipulation and photocoagulation effect that may have a positive influence on both bone remodeling and soft tissue healing. This study aims to evaluate the effectiveness of the utilization of diode laser photocoagulation with immediate implant placement and customized healing abutment in the maxillary esthetic zone.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with non-restorable maxillary teeth in the aesthetic zone are indicated for extraction and subsequent immediate implant placement, including those with:
  • •A severely carious tooth that cannot be restored.
  • •Pulpal necrosis or irreversible pulpitis that is not amenable to endodontics.
  • •Periodontally involved teeth with grade 2 mobility or above.
  • •Teeth with root caries that can't be restored.
  • •Patients with an extraction socket Type I.
  • •A good standard of oral hygiene.

排除标准

  • •Patients with extraction socket Type II or III, with buccal plate defects.
  • •Absence of at least 2 mm of bone apical to the extraction socket
  • •tooth ankylosis.
  • •Patients with deciduous teeth.
  • •Heavy smokers.
  • •Systemic conditions
  • •History of oral or intravenous bisphosphonate therapy or any treatments with other medications that may interfere with bone metabolism within the past 12 months

研究组 & 干预措施

Immediate implant with photocoagulation

Experimental

干预措施: Diode laser and Immediate implant (Other)

结局指标

主要结局

Change in wound healing

时间窗: at 7, 14, and 21 days

The wound healing will be assessed based on Landry Wound Healing Index. The Landry Index uses a numerical score based on the assessment of four given parameters (Erythema, Edema, Wound Margin Adaptation, and Presence of Exudate). Each parameter is given a score depending on its severity, and the total score determine an overall evaluation of wound healing

Change in pain socres

时间窗: at 7, 14, and 21 days

Pain will be evaluated, using visual analogue scale (VAS) as follows: (0-1= None, 2-4= Mild, 5-7= Moderate, 8-10= Severe)

Change in implant stability

时间窗: baseline and 6 months

The base line primary Implant Stability Quotient (ISQ) will be measured during the operative stage, while the secondary stability quotient will be measured 6-months post-operative during the prosthetic phase preparation.

次要结局

  • Change in Crestal Alveolar Process width(baseline and 6 months)
  • Change in labial bone thickness(baseline and 6 months)
  • Change in esthetic of soft tissue(at 1 month)
  • Change in esthetic of soft tissue(at 1 month)
  • Change in Crestal Alveolar Process width(baseline and 6 months)
  • Change in labial bone thickness(baseline and 6 months)

研究者

发起方
Hams Hamed Abdelrahman
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hams Hamed Abdelrahman

Lecturer of Dental Public Health and biostatistical consultanat

Alexandria University

研究点 (2)

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