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临床试验/NCT07573020
NCT07573020已完成不适用

Influence of Acellular Dermal Matrix on Peri-implant Soft Tissue Phenotype and Marginal Bone Loss Following Immediate Implant Placement in Anterior Maxilla: A Randomized Controlled Clinical Trial

Mansoura University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1

研究概览

简要总结

To evaluate soft tissue augmentation using acellular dermal matrix (ADM) over immediately placed dental implants in anterior maxilla.

详细描述

This randomized clinical trial was designed to evaluate and compare the efficacy of ADM versus d-PTFE membranes in the preservation of the peri-implant hard and soft tissues in the setting of immediate implant placement on the anterior maxilla.

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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with non-restorable maxillary anterior tooth/teeth.
  • Good oral hygiene.
  • Patients' cooperation and fully capable to comply with the study protocol.
  • Age ranges from 18 to 45 years.
  • Free from history of parafunctional habits e.g. clenching and bruxism
  • Sufficient inter- arch space.

排除标准

  • Any local pathological condition that contraindicates implant placement.
  • Pregnancy.
  • Medication that affects bone healing.
  • Psychological problems.
  • Patient had undergone radiation therapy to the head and neck area in the past 12 months.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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