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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05782751
Other study ID # 6
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 1, 2019
Est. completion date August 30, 2022

Study information

Verified date March 2023
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed to compare, the effectiveness of Growth Factor Enhanced Matrix (GEM 21s) ® combined either with free connective tissue graft or collagen membrane in the treatment of Miller class II gingival recession.


Description:

Materials and Methods: Twenty sites in 10 patients, with class II Miller gingival recession were allocated randomly to be treated by (GEM 21s) ® with free connective tissue graft (groupI) or GEM 21s with collagen membrane (groupII). Plaque index, bleeding on probing, recession width, recession depth, height of keratinized tissue and digital measurements were recorded at baseline, 1, 3 and 6-months'. Probing pocket depth, clinical attachment level, gingival thickness and Radiographic parameters were recorded at baseline and 6 months'. Root coverage percentage were recorded 6 months postoperative and wound healing index were recorded at 1,3 and 6-months' post-operative .


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 30, 2022
Est. primary completion date August 30, 2022
Accepts healthy volunteers No
Gender All
Age group 25 Years to 50 Years
Eligibility Inclusion Criteria: - lack of any related medical issues that contraindicate periodontal surgery, - optimum adherence as confirmed by a positive attitude towards oral hygiene, and successfully showing up for treatment appointments. - No history of any medications in the previous six months that may interfere with periodontal surgery Gingival thickness for the selected sites should be > 1mm (as measured 2mm apical to gingival margin), - Clinical attachment level = 4mm measured from cemento-enamel junction till the deepest probing depth. Exclusion Criteria: - the presence of class V caries or restoration in the site to be treated, - previous mucogingival surgery at the selected site. - Teeth that are tilted, rotated, or have any occlusal abnormalities. - Smokers and pregnant patients were excluded from the participation.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
GROUPI
10 sites treated with Free connective tissue graft (FCTG) + growth factors enhanced matrix 21 s GEM 21S + coronally advanced flap (CAF)
GROUP II
10 sites treated withCollagen membrane + GEM 21S + coronally advanced flap (CAF)

Locations

Country Name City State
Egypt Malak Mohamed Shoukheba Tanta
Egypt Malak Yousef Mohamed Shoukheba Tanta

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recession width the distance between the mesial and distal papillae along the CEJ measured at baseline , 1, 3, and 6 months up to 6 months
Primary recession depth The distance between the CEJ and the gingival margin at the midbuccal aspect of the involved tooth measured at baseline , 1, 3, and 6 months up to 6 months
Primary Height of keratinized tissue distance from the most apical point of the free gingival margin to the mucogingival junction mid-facially measured at baseline , 1, 3, and 6 months up to 6 months
Primary Gingival thickness (Gingival biotype) measured at mid-buccal area 2 mm apical to the free gingival margin measured at baseline, and 6 months postoperatively up to 6 months
Primary radiographic measurements of facial bone level, thickness and density from cone beam CT radiography measured at baseline, and 6 months postoperative up to 6 months
Primary Percentage of root coverage according to the following formula: (RD at baseline - RD at 6 months) / RD at baseline)x100 was calculated after 6 months up to 6 months
Secondary probing pocket depth measured from gingival margin to the bottom of the pocket measured at baseline, 3, and 6 months up to 6 months
Secondary clinical attachment level measured from CEJ to the bottom of the pocket measured at baseline, 3, and 6 months up to 6 months
Secondary Digital measurements all recession areas were photographed The photos were taken by a digital camera at a fixed resolution (mega pixel) taken at baseline, 1,3,and 6 months postoperative up to 6 months
Secondary healing index recorded at 1, 3 and 6 months postoperatively (Score 1: uneventful healing while score 3: poor wound healing up to 6 months
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