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临床试验/NCT03328442
NCT03328442Unknown不适用

Evaluation of Patient Satisfaction After Root Coverage Procedure Using VISTA Technique Compared to Modified Coronally Advanced Flap Technique in Conjunction With Platelet Rich Fibrin-membrane.

Cairo University0 个研究点目标入组 16 人开始时间: 2018年3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
16
主要终点
Patient satisfaction

研究概览

简要总结

VISTA technique with PRF compared to MCAF technique with PRF to treat gingival recession

详细描述

Comparison between two techniques for root coverage divided in two groups the first (test group) VISTA technique in conjunction with PRF-membrane and the second (control group)MCAF technique in conjunction with PRF-membrane for treating Miller's class I and II gingival recession defects.

Clinical Periodontal Records will be taken at baseline, 3 months and 6 months respectively.

Visual analogue scale for pain during one week after operation. Patient satisfaction record using questionnaire after 6 months.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age (18-55) Miller's classI and II multiple GR width of KG>2 mm

排除标准

  • •Systemic diseases Poor oral hygiene Smoking Patient allergy Miller's class III and IV

研究组 & 干预措施

Vista technique

Experimental

The vista technique with PRF membrane uses a Vestibular incision subperiosteal tunnel access in combination with Platelet rich fibrin membrane to treat gingival recession defects.

干预措施: VISTA Technique (Procedure)

modified coronally advanced flap

Active Comparator

A modified coronally advanced flap utilising Platelet rich fibrin membrane to treat gingival recession defects.

干预措施: modified coronally advanced flap (Procedure)

结局指标

主要结局

Patient satisfaction

时间窗: after 6 months

Using a questionnaire which are designed in a dichotomous fashion (yes or no ) and calculated by percentage of answering yes. it not a scale, the following questions will be asked to the patients; 1. did you feel pain in spite of the medication prescribed? 2. did you perceive the course of healing unexpected restriction? 3. did you experience any remaining symptoms of parasethesia? 4. would you described the under taken effort as reasonable? 5. have your expectations been fulfilled?

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

Mohamed Salah salaheldin

Assistant lecturer faculty of dentistry Nahda university

Cairo University

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