跳至主要内容
临床试验/NCT03219944
NCT03219944Unknown不适用

Clinical Evaluation of Platelet Rich Fibrin Versus Subepithelial Connective Tissue Graft for Soft Tissue Augmentation Around Implant in the Aesthetic Zone: A Randomized Control Clinical Trial

Cairo University2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2017年8月15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
16
试验地点
2
主要终点
Crestal bone resorption

研究概览

简要总结

Soft tissue biotype is a critical factor for success of implant in the esthetic zone . Different soft tissue augmentation techniques have been employed to increase soft tissue thickness such as: autogenous grafts, allografts, xenografts and living cellular construct (LCC). Studies showed that, allografts and xenografts were inferior when compared with autogenous graft . However, few studies were conducted to evaluate the efficacy of soft tissue augmentation with platelet rich fibrin in order to overcome the patient morbidity with SCTG.

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
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with missing maxillary anterior toot teeth.
  • Thin gingival biotype.
  • Adequate inter-arch space for placement of the implant prosthetic part.
  • Good oral hygiene where gingival index is (0, 1) (Loe and Silness 1963).

排除标准

  • Patient with medical condition that is contraindicated with the surgical procedure
  • Patients receiving treatment that affect the healing ability.
  • Patients with local pathological defects related to the area of interest.
  • Smokers or pregnant women.
  • Patients with parafunctional habits that may jeopardize the implant longevity and affect the results of the study.

研究组 & 干预措施

sub epithelial connective tissue graft

Active Comparator

The connective tissue graft will be harvested from the palate. Then the SCTG will be placed over the recipient site extending palataly and sutured.

干预措施: sub epithelial connective tissue graft (Procedure)

Platelet Rich Fibrin for soft tissue augmentation

Experimental

blood will be drawn from the patient vein for PRF. The blood sample will be centrifuged for 10-12 min. PRF membrane is obtained

干预措施: Platelet Rich Fibrin (Procedure)

结局指标

主要结局

Crestal bone resorption

时间窗: 6 months

measured mesially and distally using periapical xray in mm

次要结局

未报告次要终点

研究者

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

may mohamed kamal

master student

Cairo University

研究点 (2)

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