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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04966208
Other study ID # FDBSUREC/08042021/FA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date June 15, 2021

Study information

Verified date July 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Coronally the advanced flap is considered a predictable treatment of gingival recession but in certain situations, it needs a filler like subperiosteal connective tissue graft (CTG) which is considered as the gold standard treatment approach. This randomized controlled trial compares the clinical benefits and effectiveness of a xenogenic collagen matrix (mucoderm, botiss, dental, Berlin, Germany) as a filler to the subperiosteal connective tissue graft (CTG).


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date June 15, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - -The selected patients for this study are non-smokers, aged 18-60 years with multiple gingival recession (Miller class 1, or 2.) for more than two adjacent affected teeth with plaque score less than 25% Exclusion Criteria: - -Patients with systemic complications, psychological problems, parafunctional habits, or patients presented with Mal-posed teeth, hypermobile teeth, teeth with Miller class 3 gingival recession were excluded from this study.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
xenogeneic collagen matrix
xenogeneic collagen matrix called mucoderm used for root coverage for treatment of gingival recession instead of harvesting from the patients connective tissue

Locations

Country Name City State
Egypt Assiut University Assuit

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The zone of keratinized gingiva The distance from the tip of the papilla to the mucogingival junction minus the probing depth measured in mm using graduated periodontal probe. 6 months after the surgery
Secondary Periodontal probing depth measured from the gingival margin to the depth of the gingival sulcus in six sites per tooth and measured in mm. 6 months after the surgery
Secondary Clinical attachment loss measured from the cementoenamel junction to the depth of the sulcus in six sites per tooth and measured in mm. 6 months after the surgery
Secondary Gingival recession The depth measured from the gingival margin to the cementoenamel junction in mm. 6 months after the surgery
Secondary Patient satisfaction of the esthetics measured using the visual analog scale. 6 months
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