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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04561947
Other study ID # 2017-82-09/08
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date July 30, 2018

Study information

Verified date September 2020
Source Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized controlled clinical study aimed to evaluate the success of the combination of tunnel technique and concentrated growth factor membrane for root coverage in treating multiple gingival recessions and compare with the gold standard connective tissue graft.


Description:

The study included 108 defects in 40 patients with Miller Class I and II gingival recession. Gingival recession defects were randomly divided into two groups. Tunnel technique + connective tissue graft was applied to 20 patients in the control group (51 defects) and tunnel technique + concentrated growth factor membrane was applied to 20 patients in the test group (57 defects). The results at baseline and 6 months were evaluated for the following clinical parameters: Mean root coverage, complete root coverage, probing depth, clinical attachment level, gingival recession depth, gingival recession width, keratinized tissue width and gingival thickness.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 30, 2018
Est. primary completion date July 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age =18 years

- periodontally and systemically healthy

- presence of Miller I or II class gingival recession defect in at least two teeth on the buccal aspect of incisors, canine and premolar teeth (= 2 mm in depth)

- gingival thickness = 0.8 mm 2 mm apical to the gingival margin

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

- full-mouth plaque score (FMPS) =20%.

Exclusion Criteria:

- smoking

- contraindications for surgical periodontal treatment

- presence of recession defects associated caries, restoration and furcation problems

- use of systemic antibiotics for any reason in the last 3 months.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Tunnel technique
After local anesthesia, the exposed root surfaces were mechanically treated with curettes. A tunnelling knives were used to prepare a split-thickness flap and create a continuous tunnel in the buccal soft tissues, following the intrasulcular incision with a #69 microblade. Split-thickness flap preparation was performed to beyond the mucogingival junction with supraperiosteal dissection by placing the tunneling knives to the soft tissue. This process was repeated by entering through the sulcus of each tooth. After the elevation of the flap, a papilla elevator placed under the flap was entered through the sulcus to mobilize the papilla, the periosteum at the base of the papilla was cut, and the full-thickness flap was elevated.
Connective tissue graft
CTG was harvested using the de-epithelialized connective tissue graft technique. The epithelial tissue on the outer surface of the graft was removed with a 15 blade and a 1-mm-thick graft was obtained.
Other:
Concentrated growth factor membrane
Intravenous blood samples were collected in without anticoagulant 10-mL tubes and immediately centrifuged in a CGF centrifuge machine using a program with the following features: 30 ? acceleration, 2 min at 2700 rpm, 4 min at 2400 rpm, 4 min at 2700 rpm, 3 min at 3000 rpm, and 36 ? deceleration and stop. After centrifugation, four layers were formed in the tube: the serum layer at the top, the second buffy coat layer, the third CGF layer containing GF and unipotent stem cells, and the red blood cell layer at the bottom. The resulting CGF was removed from the tube and separated from the red blood cell layer using microsurgical scissors.

Locations

Country Name City State
Turkey Bulent Ecevit U. Zonguldak

Sponsors (1)

Lead Sponsor Collaborator
Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complete root coverage Change from baseline in percentage of complete root coverage at 6th months. Six months
Secondary Mean root coverage Change from baseline in percentage of root coverage at 6th months. Six months
Secondary Probing depth Change from baseline in probing depth at 6th months. The distance between the sulcus base and the gingival margin the midbuccal aspect of the teeth Six months
Secondary Clinical attachment level The changes in clinical attachment level after 6th months. Distance between the sulcus base and the CEJ in the midbuccal aspect of the teeth Six months
Secondary Gingival recession depth The changes in gingival recession depth after 6th months. Distance between the gingival margin at the deepest point of recession Six months
Secondary Gingival recession width The changes in gingival recession width after 6th months. Horizontal distance between the mesial and distal margin of the recession defect at the CEJ Six months
Secondary Keratinized tissue width The changes in keratinized tissue width after 6th months. Distance between the gingival margin and the mucogingival junction Six months
Secondary Gingival thickness The changes in gingival thickness after 6th months. Measured midbuccally from 2 mm apical to the gingival margin with a No: 20 endodontic spreader Six months
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