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

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Gingival Recession

Treatments

Procedure: modified coronally advanced flap
Procedure: VISTA Technique

Study type

Interventional

Funder types

Other

Identifiers

NCT03328442
CEBD-CU-2017-10-30

Details and patient eligibility

About

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

Full 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.

Enrollment

16 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

16 participants in 2 patient groups

Vista technique
Experimental group
Description:
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.
Treatment:
Procedure: VISTA Technique
modified coronally advanced flap
Active Comparator group
Description:
A modified coronally advanced flap utilising Platelet rich fibrin membrane to treat gingival recession defects.
Treatment:
Procedure: modified coronally advanced flap

Trial contacts and locations

0

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Central trial contact

Hani M Elnahass, PhD; Mohamed S Saleh, Master

Data sourced from clinicaltrials.gov

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