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Patient Satisfaction After Root Coverage Using VISTA Technique Compared to MCAF Technique With PRF.

Not Applicable
Conditions
Gingival Recession
Interventions
Procedure: VISTA Technique
Procedure: modified coronally advanced flap
Registration Number
NCT03328442
Lead Sponsor
Cairo University
Brief Summary

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

Detailed Description

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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Age (18-55) Miller's classI and II multiple GR width of KG>2 mm
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Exclusion Criteria
  • Systemic diseases Poor oral hygiene Smoking Patient allergy Miller's class III and IV
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vista techniqueVISTA TechniqueThe vista technique with PRF membrane uses a Vestibular incision subperiosteal tunnel access in combination with Platelet rich fibrin membrane to treat gingival recession defects.
modified coronally advanced flapmodified coronally advanced flapA modified coronally advanced flap utilising Platelet rich fibrin membrane to treat gingival recession defects.
Primary Outcome Measures
NameTimeMethod
Patient satisfactionafter 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?

Secondary Outcome Measures
NameTimeMethod
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