Gingival Recession Clinical Trial
Official title:
Clinical Evaluation of Combined Surgical/ Restorative Treatment of Gingival Recession-type Defects Using Different Restorative Materials
Verified date | May 2016 |
Source | Gazi University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Turkey: Ministry of Health |
Study type | Interventional |
Background: The aim of this study was to evaluate the treatment of multiple gingival
recessions associated with non-carious cervical lesions (NCCL) using a modified coronally
advanced flap in combination with a sub-epithelial connective tissue graft (SCTG) on
restored root surfaces.
Methods: Twenty-three systemically healthy subjects, who were positive for the presence of
three cervical lesions associated with gingival recessions in three different adjacent
teeth, were enrolled in the study. The NCCL were each restored prior to surgery by using one
of three different materials: composite resin (group 1), resin-modified glass ionomer cement
(group 2) or giomer (group 3). The defects were treated with SCTG. Clinical measurements,
including plaque index (PI), bleeding on probing (BOP), relative recession height (rRH),
probing depth (PD), cervical lesion height (CLH), relative clinical attachment level (rCAL),
keratinized tissue height (KTH), keratinized tissue thickness (KTT), percentage of root
coverage (RC), and percentage of cervical lesion height coverage (CLHC) were recorded at
baseline, 3 and 6 months, and 1 year postoperatively.
Status | Completed |
Enrollment | 18 |
Est. completion date | February 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: 1. Positive for the presence of three cervical lesions associated with multiple gingival recessions in three different adjacent teeth excluding molars; 2. Miller Class I gingival recession defect (=2 and =5 mm) associated with buccal NCCL (lesion depth 1-2 mm); 3. Non-smoker; 4. Systemically and periodontally healthy; 5. Not taking medications known to interfere with periodontal tissue health or healing; 6. Probing depth (PD)=3 mm; 7. Presence of =1 mm highly keratinized tissue apical to the root exposure, and presence of =0.8 mm-thick gingival tissue; 8. Absence of non-vital teeth, caries or restorations on cervical areas, severe occlusal interferences and previous surgery in the area. Exclusion Criteria: - inflammatory periodontal disease; previous surgical attempt to correct gingival recession; systemic disease or severe immune deficiency; coagulation defect or current anticoagulation treatment; addiction to drugs; inability or unwillingness to complete the trial; lack of linguistic skills; psychiatric disorders; refusal to sign the informed consent form; pregnancy; molar or premolar teeth with furcation involvement. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Gazi University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | relative gingival recession height | measured as distance from the most apical point of gingival margin to the incisional border of the tooth | one year post-op | No |
Secondary | keratinized tissue width | measured from most apical point of the gingival margin to the mucogingival junction | one year | No |
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