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Ozonized In-office and Domiciliary Gels vs Chlorhexidine Gel 1% for the Management of Peri-implant Mucositis Sites

Primary Purpose

Peri-implant Mucositis

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Ozoral Pro and Ozoral gel administration
Curasept chlorhexidine gel 1%
Sponsored by
University of Pavia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peri-implant Mucositis

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Sites / Locations

  • Unit of Dental Hygiene - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Paediatrics - University of Pavia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Peri-implant mucositis sites

Contralateral peri-implant mucositis sites

Arm Description

Peri-implant mucositis sites will be randomly assigned to ozone treatment.

Contralateral peri-implant mucositis sites with respect to those treated with ozone will be assigned to chlorhexidine treatment.

Outcomes

Primary Outcome Measures

Change in Bleeding on Probing (BOP%)
Dichotomous scoring (yes/no) of bleeding sites
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
Change in Suppuration (%)
Dichotomous scoring (yes/no) of suppurating sites
Change in marginal mucosa condition
Scoring criteria: 0: normal mucosa minimal inflammation with color change and minor edema moderate inflammation with redness, edema and glazing severe inflammation with redness, edema, ulceration and spontaneous bleeding without probing
Change in mucosal margin
Dichotomous scoring (migrated/non migrated)
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.
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
Change in Bleeding Score (BS - Mombelli et al.)
Scoring criteria: 0: no bleeding isolated visible spots blood forms a confluent red line on the mucosal margin profuse and copious bleeding

Secondary Outcome Measures

Full Information

First Posted
February 16, 2022
Last Updated
October 6, 2022
Sponsor
University of Pavia
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1. Study Identification

Unique Protocol Identification Number
NCT05256914
Brief Title
Ozonized In-office and Domiciliary Gels vs Chlorhexidine Gel 1% for the Management of Peri-implant Mucositis Sites
Official Title
Ozonized In-office and Domiciliary Gels vs Chlorhexidine Gel 1% for the Management of Peri-implant Mucositis Sites: a Randomized Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
February 27, 2022 (Actual)
Primary Completion Date
October 3, 2022 (Actual)
Study Completion Date
October 6, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pavia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.
Detailed Description
This is a split-mouth randomized controlled clinical trial (RCT). 30 patients is expected to be enrolled. 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), and after 6 months (T3). At T2 and T3, professional hygiene will be performed again. At each recall session, the following periodontal clinical indices were collected using a probe on each peri-implant site: BOP (bleeding on probing) and GBI (gingival bleeding index) Conditions of the marginal mucosa (swelling and erythema) Suppuration Migration of the marginal mucosa PD (probing depth) PI (plaque index) BS (bleeding score)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peri-implant Mucositis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Split-mouth design
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Gels concealed
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Peri-implant mucositis sites
Arm Type
Experimental
Arm Description
Peri-implant mucositis sites will be randomly assigned to ozone treatment.
Arm Title
Contralateral peri-implant mucositis sites
Arm Type
Experimental
Arm Description
Contralateral peri-implant mucositis sites with respect to those treated with ozone will be assigned to chlorhexidine treatment.
Intervention Type
Other
Intervention Name(s)
Ozoral Pro and Ozoral gel administration
Intervention Description
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).
Intervention Type
Other
Intervention Name(s)
Curasept chlorhexidine gel 1%
Intervention Description
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).
Primary Outcome Measure Information:
Title
Change in Bleeding on Probing (BOP%)
Description
Dichotomous scoring (yes/no) of bleeding sites
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in Gingival Bleeding Index (GBI%)
Description
Quantitative assessment (percentage) of the bleeding sites (6 per tooth in total). Formula = n ° bleeding sites / n ° probed sites x100
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in Suppuration (%)
Description
Dichotomous scoring (yes/no) of suppurating sites
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in marginal mucosa condition
Description
Scoring criteria: 0: normal mucosa minimal inflammation with color change and minor edema moderate inflammation with redness, edema and glazing severe inflammation with redness, edema, ulceration and spontaneous bleeding without probing
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in mucosal margin
Description
Dichotomous scoring (migrated/non migrated)
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in Probing Depth (PD)
Description
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.
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in Plaque Index (PI% - O' Leary Index)
Description
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
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)
Title
Change in Bleeding Score (BS - Mombelli et al.)
Description
Scoring criteria: 0: no bleeding isolated visible spots blood forms a confluent red line on the mucosal margin profuse and copious bleeding
Time Frame
Baseline (T0), after 1 (T1), 3 (T2) and 6 months (T3)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Scribante, DDS, PhD, MS
Organizational Affiliation
University of Pavia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Unit of Dental Hygiene - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Paediatrics - University of Pavia
City
Pavia
State/Province
Lombardy
ZIP/Postal Code
27100
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data are available upon motivated request to the Authors.

Learn more about this trial

Ozonized In-office and Domiciliary Gels vs Chlorhexidine Gel 1% for the Management of Peri-implant Mucositis Sites

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