Chronic Inflammatory Gingival Enlargement, Gingival Enlargement, Gingival Hyperplasia
Conditions
Keywords
Ozone Therapy, Gingivectomy, Wound Healing, Periodontal Surgery, Superficial Cell Index, Split-Mouth Clinical Trial
Brief summary
Gingival enlargement caused by chronic inflammation may require surgical intervention when non-surgical periodontal therapy is insufficient. Gingivectomy and gingivoplasty are commonly performed procedures to remove excessive gingival tissue and restore normal gingival contour. However, postoperative wound healing may be affected by factors such as microbial contamination and the inflammatory response. Medical ozone therapy has antimicrobial, anti-inflammatory, and biostimulatory properties that may enhance tissue regeneration and accelerate wound healing. The aim of this randomized split-mouth clinical trial is to evaluate the effect of adjunctive gaseous ozone therapy on wound healing following gingivectomy/gingivoplasty in individuals with chronic inflammatory gingival enlargement. Twenty-four systemically healthy participants diagnosed with chronic inflammatory gingival enlargement will be included. Surgical sites will be randomly assigned in a split-mouth design to either the test group (gingivectomy/gingivoplasty with adjunctive gaseous ozone application) or the control group (gingivectomy/gingivoplasty alone). Clinical periodontal parameters (Plaque Index, Gingival Index, Bleeding on Probing, Probing Pocket Depth, and Clinical Attachment Level) will be assessed at baseline and post-operative Day 21. Histopathological outcomes (Superficial Cell Index and Keratinization Index) will be evaluated at baseline and on post-operative Days 1, 3, 7, and 21. The results of this study are expected to provide clinical and histopathological evidence regarding the potential benefits of adjunctive ozone therapy in periodontal wound healing.
Detailed description
Chronic inflammatory gingival enlargement is a condition characterized by an increase in gingival volume due to inflammatory changes associated with dental plaque. Non-surgical periodontal therapy is the primary treatment approach; however, in some cases, surgical intervention such as gingivectomy or gingivoplasty is required to eliminate excess gingival tissue and restore gingival architecture. Gingivectomy/gingivoplasty creates a surgical wound surface that is exposed to the oral environment and microbial flora. Therefore, the healing process may be influenced by several biological and environmental factors. Adjunctive therapeutic approaches that enhance wound healing and reduce microbial contamination may improve clinical outcomes following periodontal surgery. Medical ozone therapy, consisting of a controlled mixture of oxygen (O₂) and ozone (O₃), has antimicrobial, anti-inflammatory, and immunomodulatory properties. It has also been suggested to stimulate fibroblast activity, enhance tissue oxygenation, and promote growth factor release, potentially accelerating tissue regeneration and wound healing. The present study is designed as a single-center, randomized, split-mouth clinical trial with blinded outcome assessment to investigate the effect of adjunctive gaseous ozone therapy on wound healing following gingivectomy/gingivoplasty in patients with chronic inflammatory gingival enlargement. A total of 24 systemically healthy individuals aged between 18 and 40 years diagnosed with chronic inflammatory gingival enlargement will be included. Following non-surgical periodontal therapy and oral hygiene instruction, gingivectomy/gingivoplasty will be performed under local anesthesia. Surgical sites will be randomly assigned using a coin-toss method in a split-mouth design to either the test group (gingivectomy/gingivoplasty with adjunctive gaseous ozone application) or the control group (gingivectomy/gingivoplasty alone). In the test group, gaseous ozone will be applied to the surgical wound area using a dedicated probe for one minute per tooth according to the manufacturer's instructions. Ozone application will be repeated at 24 hours and on post-operative Day 3. Clinical periodontal parameters (Plaque Index \[PI\], Gingival Index \[GI\], Bleeding on Probing \[BOP\], Probing Pocket Depth \[PPD\], and Clinical Attachment Level \[CAL\]) will be assessed at baseline and on post-operative Day 21. Exfoliative cytology samples will be obtained from the wound area at baseline and on post-operative Days 1, 3, 7, and 21. Histopathological evaluation will be performed to determine the Superficial Cell Index (SCI) and Keratinization Index (KI), which are indicators of epithelial maturation and wound healing. The findings of this study are expected to provide clinical and histopathological evidence regarding the potential benefits of adjunctive ozone therapy in periodontal wound healing and may support its use as an adjunctive treatment in periodontal surgical procedures.
Interventions
Gaseous ozone is applied to the surgical wound area using an ozone delivery probe for 1 minute per tooth following gingivectomy/gingivoplasty. The application is repeated at 24 hours and on post-operative Day 3.
Gingivectomy/gingivoplasty is performed under local anesthesia without any additional adjunctive treatment.
Sponsors
Study design
Masking description
This study was designed as a double-blind clinical trial. Participants and outcome assessors were blinded to the treatment allocation. Histopathological evaluation and statistical analyses were performed by investigators who were unaware of group assignments.
Intervention model description
This study uses a randomized split-mouth design. Surgical sites within the same participant are randomly assigned to either the test group (gingivectomy/gingivoplasty with adjunctive gaseous ozone application) or the control group (gingivectomy/gingivoplasty alone).
Eligibility
Inclusion criteria
* Systemically healthy individuals * Patients diagnosed with chronic inflammatory gingival enlargement * Presence of gingival enlargement affecting the maxillary or mandibular anterior region * Symmetrical involvement of at least six teeth * No clinical attachment loss * Ability to maintain adequate oral hygiene following non-surgical periodontal therapy * No pregnancy or lactation
Exclusion criteria
* Presence of systemic diseases that may affect wound healing * Current orthodontic treatment * Smoking or alcohol use * Use of medications affecting periodontal tissues within the last two months * Inability to maintain adequate oral hygiene
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Superficial Cell Index (SCI) | Baseline, and post-operative Days 1, 3, 7, and 21 | Evaluation of epithelial cell maturation and wound healing using exfoliative cytology based on the analysis of at least 200 cells per smear. |
| Keratinization Index (KI) | Baseline, and post-operative Days 1, 3, 7, and 21 | Assessment of epithelial keratinization during the wound healing process using exfoliative cytology. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Plaque Index (PI) | Baseline and post-operative Day 21 | Measurement of dental plaque accumulation. |
| Gingival Index (GI) | Baseline and post-operative Day 21 | Assessment of gingival inflammation severity. |
| Bleeding on Probing (BOP) | Baseline and post-operative Day 21 | Evaluation of gingival bleeding following periodontal probing. |
| Probing Pocket Depth (PPD) | Baseline and post-operative Day 21 | Measurement of periodontal pocket depth in millimeters. |
| Clinical Attachment Level (CAL) | Baseline and post-operative Day 21 | Assessment of periodontal attachment level in millimeters. |
Countries
Turkey (Türkiye)