Ozonized In-office and Domiciliary Gels vs Chlorhexidine Gel 1% for the Management of Peri-implant Mucositis Sites
1 other identifier
interventional
30
1 country
1
Brief Summary
This is a split-mouth randomized controlled clinical trial (RCT). After signing the informed consent, patients satisfying the inclusion criteria will undergo supragingival and subgingival professional oral hygiene of both arches performed with ultrasonic instrumentation with PEEK inserts, manual instrumentation with titanium curettes and air polishing with glycine powder. After that, the following treatment will be randomly assigned:
- Ozoral Pro and Ozoral gel administration and home application for 2 peri-implant mucositis sites.
- Curasept chlorhexidine gel 1% administration and domiciliary application for 14 days for 2 peri-implant contralateral sites. The study will last 6 months. Patients will be visited at: T0, after 1 month from T0 (T1), after 3 months (T2), after 6 months (T3). Professional hygiene will be performed again at T2 and T3. At each recall session, the following periodontal clinical indices were collected using a probe on each peri-implant site: BOP, GBI, conditions of the marginal mucosa (swelling and erythema), suppuration, migration of the marginal mucosa, PD, PI ,BS.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 16, 2022
CompletedFirst Posted
Study publicly available on registry
February 25, 2022
CompletedStudy Start
First participant enrolled
February 27, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 3, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
October 6, 2022
CompletedOctober 7, 2022
October 1, 2022
7 months
February 16, 2022
October 6, 2022
Conditions
Outcome Measures
Primary Outcomes (8)
Change in Bleeding on Probing (BOP%)
Dichotomous scoring (yes/no) of bleeding sites
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in Gingival Bleeding Index (GBI%)
Quantitative assessment (percentage) of the bleeding sites (6 per tooth in total). Formula = n ° bleeding sites / n ° probed sites x100
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in Suppuration (%)
Dichotomous scoring (yes/no) of suppurating sites
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in marginal mucosa condition
Scoring criteria: 0: normal mucosa 1. minimal inflammation with color change and minor edema 2. moderate inflammation with redness, edema and glazing 3. severe inflammation with redness, edema, ulceration and spontaneous bleeding without probing
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in mucosal margin
Dichotomous scoring (migrated/non migrated)
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in Probing Depth (PD)
Evaluation (in mm) of the depth of the gingival sulcus, through a millimeter periodontal probe; it is detected from the gingival margin to the bottom of the gingival sulcus or periodontal pocket, evaluated at 6 sites.
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in Plaque Index (PI% - O' Leary Index)
Evaluation of the presence of plaque on the 4 surfaces of teeth on the total amount of dental surfaces. Formula = n ° sites with plaque / total n ° of dental surfaces x100
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Change in Bleeding Score (BS - Mombelli et al.)
Scoring criteria: 0: no bleeding 1. isolated visible spots 2. blood forms a confluent red line on the mucosal margin 3. profuse and copious bleeding
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Study Arms (2)
Peri-implant mucositis sites
EXPERIMENTALPeri-implant mucositis sites will be randomly assigned to ozone treatment.
Contralateral peri-implant mucositis sites
EXPERIMENTALContralateral peri-implant mucositis sites with respect to those treated with ozone will be assigned to chlorhexidine treatment.
Interventions
Peri-implant mucositis sites will receive in-office Ozoral Pro administration after non-surgical therapy. Patients will use Ozoral Gel for the domiciliary administration once a day for 14 days after the visits (no rinsing and eating for 30 minutes after gel application).
Peri-implant mucositis sites will receive in-office Curasept chlorhexidine gel 1% administration after non-surgical therapy. Patients will use chlorhexidine gel 1% for the domiciliary application once a day for 14 days after the visits (no rinsing and eating for 30 minutes after gel application).
Eligibility Criteria
You may qualify if:
- age 18-70 years
- presence of 2 peri-implant mucositis sites per side (left and right) with PD \> 5 mm
- no systemic, metabolic and autoimmune disease
- compliant patients
You may not qualify if:
- neurologic, psychiatric and mental diseases
- patients taking bisphosphonates in the last 12 months
- patients taking antibiotics during the study
- pregnant and breastfeeding women
- patients undergoing anticancer treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Unit of Dental Hygiene - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Paediatrics - University of Pavia
Pavia, Lombardy, 27100, Italy
Study Officials
- PRINCIPAL INVESTIGATOR
Andrea Scribante, DDS, PhD, MS
University of Pavia
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Gels concealed
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor, Principal Investigator
Study Record Dates
First Submitted
February 16, 2022
First Posted
February 25, 2022
Study Start
February 27, 2022
Primary Completion
October 3, 2022
Study Completion
October 6, 2022
Last Updated
October 7, 2022
Record last verified: 2022-10
Data Sharing
- IPD Sharing
- Will not share
Data are available upon motivated request to the Authors.