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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04181892
Other study ID # CukurovaU-PER-I
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date September 1, 2019

Study information

Verified date November 2019
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim: The aim of this study was to compare the root coverage and aesthetic results of CAF+ CTG positioned apical to the CEJ (CAF+CTG-ACEJ) with CAF+CTG positioned on the CEJ (CAF+CTG-CEJ) for treating isolated gingival recession defects.

Methods: Thirthy-eight patients with Miller class I and II gingival recessions were enrolled. 19 patients were randomly assigned to the CAF+CTG-ACEJ group or CAF+CTG-CEJ group. Clinical and aesthetical evaluations were made at 6 months.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date September 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 60 Years
Eligibility Inclusion Criteria:

- 19 years of age,

- Periodontally and systemically healthy,

- FMPS and FMBS <15%,

- Presence of Miller Class I/II GR defect (=3 mm in depth) at the buccal aspect of incisors and canines,

- Presence of identifiable CEJ (step =1 mm at CEJ level and/or presence of a root irregularity/abrasion with identifiable CEJ, was accepted),

- No previous periodontal surgery.

Exclusion Criteria:

- Smoking,

- Contraindications for surgery,

- Presence of recession defects associated with caries, deep abrasion, restoration or pulpal pathology.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Coronally advanced flap + connective tissue graft
connective tissue graft covered by a coronally advanced flap with connective tissue graft apical of the cementoenamel junction level

Locations

Country Name City State
Turkey Cukurova University Faculty of Dentistry Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gingival Recession depth in millimeters measured from the cemento-enamel junction to the gingival margin 6 months
Primary keratinized tissue height in millimeters measured from the mucogingival junction to the gingival margin 6 months
Primary aesthetic evaluation assesed by visual analog scale 6 months
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