Gingival Recession Clinical Trial
Official title:
Effectiveness and Predictability of Titanium-Prepared Platelet-Rich Fibrin for the Management of Multiple Gingival Recessions
Objective: Titanium-prepared platelet-rich fibrin (T-PRF) is activated with titanium, which
results in a more mature and aggregated form than PRF. In our previous studies, we
established that the fibrin carpet formed with titanium had a firmer network structure, and
longer resorption time in the tissue than the fibrin carpet formed with glass. The purpose
of this randomized controlled clinical trial is to compare the effects of autogenous T-PRF
and CTG.
Materials and methods: A total 114 Miller Class I/II gingival recessions with abrasion
defects will be treated either T-PRF (63 teeth) or CTG (51 teeth) using a modified tunnel
technique. Clinical periodontal indexes, keratinized tissue (KTW), gingival thickness (GT)
and recession depth (RD) will be recorded before surgery and at 6 and 12-month follow-up
examinations. The Visual Analog Scale and healing index scores will be assessed.
A total of 34 patients will be informed in detail about the risks and benefits of each step
of the study, and their signed consents will be obtained.
These clinical assessments will be done:
1. Plaque Index and Gingival Index In case of multiple gingival recessions, plaque index
and gingival index will be obtained from the three dental points as mesial, distal and
vestibule midpoints; plaque index will be calculated according to Sillnes&Löe criteria,
whereas gingival index will be calculated according to Löe&Silness criteria.
2. Periodontal Pocket Depth In case of multiple gingival recessions, the distance between
the pocket base and free gingival margin will be measured separately for each tooth
with the assistance of periodontal Williams probe through the midpoint of vestibule.
3. Recession Width Periodontal probe will be horizontally placed on the enamel-cement
border and the measurement will be recorded.
4. Recession Depth The defect distance will be measured vertically from the enamel-cement
conjunction of the tooth to the very apical aspect of the gingival margin using
periodontal probe and recorded in millimeters.
5. Clinical Attachment Level The clinical attachment level (CAL) will be measured by
periodontal probe through the midpoint of vestibule as the distance between gingiva
base and enamel-cement border and recorded in millimeters.
6. Keratinized Tissue Width The distance between gingival margin and alveolar mucosa will
be measured in millimeters. A solution consisted of 10% potassium iodide and 5% iodine
will be applied onto the gingiva and alveolar mucosa with a cotton pellet. This
solution stains the glycogen-rich alveolar mucosa darker than the keratinized tissue
and allows keratinized gingival mucosa to be exposed more clearly.
7. Gingival Thickness This measurement will be performed in the relevant area by No. 15
endodontic spreader under topical anesthesia. The spreader will be placed perpendicular
to the gingiva through approximately 1.5 mm apical aspect of the gingival margin,
pushed forward until obtaining bone support, and fixed with a disc. The distance
between the disc and the tip of endochuck will be measured by a digital caliper with a
sensitivity of 0.1 mm.
8. Measurement of CTG Thickness Fat and glandular tissue and band-shape epithelium on the
CTG, which will be derived from the maxillary palate, will be removed by a scissor. The
graft, which will be placed onto a sterile, metal smooth surface, will be fixed through
its mesial, distal and middle aspects by a No. 15 endodontic spreader with the
assistance of a disc and then measured by digital caliper. The mean graft thickness
will be calculated as the arithmetic mean of the values measured.
9. Measurement of T-TRF Membrane Thickness Two thrombocyte rich platelets taken from the
tubes that have been centrifuged will be separated from the serum at room temperature
in sterile gauze and will be turned into membranes. They will be measured by digital
caliper as two-layer similar to the measurement of connective tissue thickness, and the
values will be recorded..
VAS Assessment On the postoperative Day 1, 3 and 7, the patients will be asked to complete a
chart where they can rate subjective complaints of pain, burning sensation and discomfort in
the surgery site between 0 (none) and 100 (very severe).
Wound Healing Index While removing the sutures two weeks after surgery, the physician will
evaluate wound healing according to the Huang criteria separately for each tooth; Score 1:
Problem-free wound healing without gingival edema, erythema, suppuration, or dehiscence of
the flap margins.
Score 2. Problem-free wound healing with mild gingival edema, erythema, patient discomfort
and flap dehiscence without suppuration.
Score 3. Poor wound healing with severe gingival edema, erythema, suppuration, patient
discomfort and flap dehiscence.
Calculation of Root Surface Coverage Ratio This ratio is presented as percentage (%) and
evaluated in the 6th and 12th months.
Preoperative recession depth - Postoperative recession depth X 100 % Preoperative recession
depth
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