search
Back to results

Surgical Access Combined With Systematically Administered Antibiotics in the Treatment of Peri-implantitis

Primary Purpose

Peri-Implantitis

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Open flap debridement
Er: YAG irradiation
Metronidazole
Amoxicillin
Placebos
Sponsored by
University of Guarulhos
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peri-Implantitis focused on measuring peri-implantitis, open flap debridement, Er:YAG irradiation, metronidazole, amoxicillin, microbiota

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18-70 years of age;
  • in general good health,
  • at least one dental implant in function for at least one year with untreated peri-implantitis defined as: presence of bleeding and/or suppuration on gentle probing, probing depths (PD) ≥ 6mm, and bone levels ≥3mm apical of the most coronal portion of the intraosseous part of the implant.

Exclusion Criteria:

  • subjects with ≥6 sites with PD ≥5mm;
  • individuals that received periodontal treatment within three months prior to entering the study;
  • inability to perform proper supramucosal and supragingival plaque control (e.g., due to improper restoration design or lack of skills);
  • poorly adapted implant-supported restoration;
  • diabetes;
  • pregnancy;
  • nursing;
  • history of allergies to metronidazole and/or amoxicillin, or any other ingredient of oral care products;
  • alcohol or drug abuse;
  • any systemic diseases that could affect post-operative healing or that required antibiotic premedication for routine dental therapy;
  • long-term use of mouthrinses;
  • anti-inflammatory medications;
  • any other drug that could interfere with the study outcomes within three months prior to entering the study;
  • use of antibiotics within six months prior to entering the study.

Sites / Locations

  • University of GuarulhosRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control

Test

Arm Description

Open flap debridement + Er: YAG irradiation alone + systemic placebo of metronidazole and amoxicillin thrice a day (TID) for 14 days

Open flap debridement + Er: YAG irradiation alone + systemic metronidazole (400mg) and amoxicillin (500mg) thrice a day (TID) for 14 days

Outcomes

Primary Outcome Measures

Difference between treatment groups for the change in the clinical attachment level (CAL).

Secondary Outcome Measures

Percentage of patients (and implants) reaching the following clinical endpoint for treatment: PD< 5mm, absence of BOP and no further bone loss.
Mean plaque index.
Mean gingival index.
Percentage of sites with bleeding on probing.
Percentage of sites with suppuration.
Probing depth.
Occurrence of headache obtained through a questionnaire of adverse effects.
Occurrence of vomiting obtained through a questionnaire of adverse effects.
Occurrence of diarrhea obtained through a questionnaire of adverse effects.
Occurrence of metallic taste obtained through a questionnaire of adverse effects.
Occurrence of nausea obtained through a questionnaire of adverse effects.
Occurrence of irritability obtained through a questionnaire of adverse effects.
Proportions of periodontal pathogenic bacterial species.
Counts of periodontal pathogenic bacterial species.

Full Information

First Posted
June 29, 2022
Last Updated
May 11, 2023
Sponsor
University of Guarulhos
Collaborators
ITI Foundation
search

1. Study Identification

Unique Protocol Identification Number
NCT05444218
Brief Title
Surgical Access Combined With Systematically Administered Antibiotics in the Treatment of Peri-implantitis
Official Title
Clinical and Microbiological Effects of Surgical Access Combined With Systematically Administered Antibiotics in the Treatment of Peri-implantitis: 1-year Randomized Double-blinded Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
September 10, 2023 (Anticipated)
Study Completion Date
November 5, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guarulhos
Collaborators
ITI Foundation

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 randomized clinical trial evaluates the clinical and microbiological (microbial complexes and changes in the diversity of the submucosal biofilm) effects of MTZ+AMX as adjuncts to anti-infectious surgical treatment plus Er: YAG in the treatment of peri-implantitis.
Detailed Description
Peri-implantitis is a pathological condition characterized by inflammation of peri-implant connective tissues and progressive peri-implant bone. Recently, the therapeutic protocol using non-surgical debridement associated with the combination of systemic metronidazole (MTZ) and amoxicillin (AMX) has not been shown to be effective in controlling the disease. These unfavorable results may have occurred due to the limitation in the change of the submucosal microbiological profile due to mechanical difficulties in the decontamination of the implant threads. Therefore, this randomized clinical trial (RCT) aimed to evaluate the clinical and microbiological (microbial complexes and changes in the diversity of the submucosal biofilm) effects of MTZ+AMX as adjuncts to anti-infectious surgical treatment plus Er:YAG in the treatment of peri-implantitis. Ninety-four subjects with untreated peri-implantitis are being included and will be randomly assigned to receive (i) open flap debridement plus Er:YAG irradiation alone (control), or (ii) with adjunctive systemically administered MTZ (400 mg) + AMX (500 mg) thrice a day (TID) for 14 days (test). Subjects will be monitored up to 12 months post-treatment. Submucosal biofilm samples from the deepest site of each implant with peri-implantitis will be collected in duplicate per patient: at baseline and at 3, 6 and 12 months post-therapy and analyzed by checkerboard DNA-DNA hybridization for 40 bacterial species, and at baseline, 3 and 12 months post-treatment for 16S rRNA sequencing (Ion Torrent PGM System). The primary outcome variable of this trial will be the difference between treatment groups for the change in CAL from baseline to 12 months. The significance of differences in each group (over the course of the study) will be sought using the Student's-t test; and among groups (at each time point) using either ANOVA /ANCOVA or Kruskal Wallis tests and post-hoc analyses, depending on normality of the data. Fisher's exact test will be used to compare differences in the frequency of gender. Statistical significance will be set at 5%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peri-Implantitis
Keywords
peri-implantitis, open flap debridement, Er:YAG irradiation, metronidazole, amoxicillin, microbiota

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
94 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Open flap debridement + Er: YAG irradiation alone + systemic placebo of metronidazole and amoxicillin thrice a day (TID) for 14 days
Arm Title
Test
Arm Type
Experimental
Arm Description
Open flap debridement + Er: YAG irradiation alone + systemic metronidazole (400mg) and amoxicillin (500mg) thrice a day (TID) for 14 days
Intervention Type
Procedure
Intervention Name(s)
Open flap debridement
Other Intervention Name(s)
OFD
Intervention Description
After local anesthesia (2% lidocaine with1:100,000 epinephrine), intrasulcular incisions will be performed to create a horizontal flap extending beyond the adjacent teeth and/or implants. Buccal and lingual full-thickness flaps will be dissected, and granulation tissue will be removed to expose the implant threads and bone defect. The flap will be repositioned in its original position and stabilized with interrupted sutures, which will be removed after 10 days.
Intervention Type
Other
Intervention Name(s)
Er: YAG irradiation
Intervention Description
An Er:YAG laser (Lite Touch, Light Instruments, Israel) will be used, with an irradiation energy of 20 mJ, frequency of 20 Hz, output power of 0.4 W, and an energy density of 2.76 J/cm2. An 8 mm long sapphire tip will be used in the respective handpiece and not in contact with the titanium surface, with concomitant water spray irrigation, under air 6 and water spray 6, the irradiation angle will be 90 degrees, at a focal distance of 2 mm, with spot size diameter of 1.3 mm
Intervention Type
Drug
Intervention Name(s)
Metronidazole
Other Intervention Name(s)
MTZ
Intervention Description
Metronidazole 400 mg thrice a day for 14 days in the active phase of the periodontal treatment (beginning after open flap debridement).
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Other Intervention Name(s)
AMX
Intervention Description
Amoxicillin 500 mg thrice a day for 14 days in the active phase of the periodontal treatment (beginning after open flap debridement).
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
Amoxicillin and metronidazole placebos thrice a day for 14 days in the healing phase (beginning after open flap debridement).
Primary Outcome Measure Information:
Title
Difference between treatment groups for the change in the clinical attachment level (CAL).
Time Frame
12 months.
Secondary Outcome Measure Information:
Title
Percentage of patients (and implants) reaching the following clinical endpoint for treatment: PD< 5mm, absence of BOP and no further bone loss.
Time Frame
12 months.
Title
Mean plaque index.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Mean gingival index.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Percentage of sites with bleeding on probing.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Percentage of sites with suppuration.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Probing depth.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Occurrence of headache obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Occurrence of vomiting obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Occurrence of diarrhea obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Occurrence of metallic taste obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Occurrence of nausea obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Occurrence of irritability obtained through a questionnaire of adverse effects.
Time Frame
14 days after taking antibiotic.
Title
Proportions of periodontal pathogenic bacterial species.
Time Frame
Baseline, 3, 6 and 12 months.
Title
Counts of periodontal pathogenic bacterial species.
Time Frame
Baseline, 3, 6 and 12 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-70 years of age; in general good health, at least one dental implant in function for at least one year with untreated peri-implantitis defined as: presence of bleeding and/or suppuration on gentle probing, probing depths (PD) ≥ 6mm, and bone levels ≥3mm apical of the most coronal portion of the intraosseous part of the implant. Exclusion Criteria: subjects with ≥6 sites with PD ≥5mm; individuals that received periodontal treatment within three months prior to entering the study; inability to perform proper supramucosal and supragingival plaque control (e.g., due to improper restoration design or lack of skills); poorly adapted implant-supported restoration; diabetes; pregnancy; nursing; history of allergies to metronidazole and/or amoxicillin, or any other ingredient of oral care products; alcohol or drug abuse; any systemic diseases that could affect post-operative healing or that required antibiotic premedication for routine dental therapy; long-term use of mouthrinses; anti-inflammatory medications; any other drug that could interfere with the study outcomes within three months prior to entering the study; use of antibiotics within six months prior to entering the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jamil A Shibli, Professor
Phone
+55 11 2464-1726
Email
jshibli@ung.br
First Name & Middle Initial & Last Name or Official Title & Degree
Magda Feres, Professor
Phone
+55 11 2464-1726
Email
mferes@ung.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jamil A Shibli, Professor
Organizational Affiliation
University of Guarulhos
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Guarulhos
City
Guarulhos
State/Province
São Paulo
ZIP/Postal Code
07023-070
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jamil A Shibli, Professor
Phone
+55 11 2464-1726
Email
jshibli@ung.br
First Name & Middle Initial & Last Name & Degree
Jamil A Shibli, Professor
First Name & Middle Initial & Last Name & Degree
Magda Feres, Professor
First Name & Middle Initial & Last Name & Degree
Belen Retamal-Valdes, Professor
First Name & Middle Initial & Last Name & Degree
Rafael S Siroma, PhD student
First Name & Middle Initial & Last Name & Degree
Marcelo Melo, PhD student
First Name & Middle Initial & Last Name & Degree
Michael G Vidal, PhD student

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29926955
Citation
Berglundh T, Armitage G, Araujo MG, Avila-Ortiz G, Blanco J, Camargo PM, Chen S, Cochran D, Derks J, Figuero E, Hammerle CHF, Heitz-Mayfield LJA, Huynh-Ba G, Iacono V, Koo KT, Lambert F, McCauley L, Quirynen M, Renvert S, Salvi GE, Schwarz F, Tarnow D, Tomasi C, Wang HL, Zitzmann N. Peri-implant diseases and conditions: Consensus report of workgroup 4 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. J Periodontol. 2018 Jun;89 Suppl 1:S313-S318. doi: 10.1002/JPER.17-0739.
Results Reference
background
PubMed Identifier
29926957
Citation
Schwarz F, Derks J, Monje A, Wang HL. Peri-implantitis. J Periodontol. 2018 Jun;89 Suppl 1:S267-S290. doi: 10.1002/JPER.16-0350.
Results Reference
background
PubMed Identifier
29882313
Citation
Dreyer H, Grischke J, Tiede C, Eberhard J, Schweitzer A, Toikkanen SE, Glockner S, Krause G, Stiesch M. Epidemiology and risk factors of peri-implantitis: A systematic review. J Periodontal Res. 2018 Oct;53(5):657-681. doi: 10.1111/jre.12562. Epub 2018 Jun 7.
Results Reference
background
PubMed Identifier
18828812
Citation
Shibli JA, Melo L, Ferrari DS, Figueiredo LC, Faveri M, Feres M. Composition of supra- and subgingival biofilm of subjects with healthy and diseased implants. Clin Oral Implants Res. 2008 Oct;19(10):975-82. doi: 10.1111/j.1600-0501.2008.01566.x.
Results Reference
background
PubMed Identifier
27420109
Citation
Perez-Chaparro PJ, Duarte PM, Shibli JA, Montenegro S, Lacerda Heluy S, Figueiredo LC, Faveri M, Feres M. The Current Weight of Evidence of the Microbiologic Profile Associated With Peri-Implantitis: A Systematic Review. J Periodontol. 2016 Nov;87(11):1295-1304. doi: 10.1902/jop.2016.160184. Epub 2016 Jul 15.
Results Reference
background
PubMed Identifier
25039292
Citation
Faggion CM Jr, Listl S, Fruhauf N, Chang HJ, Tu YK. A systematic review and Bayesian network meta-analysis of randomized clinical trials on non-surgical treatments for peri-implantitis. J Clin Periodontol. 2014 Oct;41(10):1015-25. doi: 10.1111/jcpe.12292. Epub 2014 Aug 11.
Results Reference
result
PubMed Identifier
31261945
Citation
Swider K, Dominiak M, Grzech-Lesniak K, Matys J. Effect of Different Laser Wavelengths on Periodontopathogens in Peri-Implantitis: A Review of In Vivo Studies. Microorganisms. 2019 Jun 29;7(7):189. doi: 10.3390/microorganisms7070189.
Results Reference
result
PubMed Identifier
25867988
Citation
Aoki A, Mizutani K, Schwarz F, Sculean A, Yukna RA, Takasaki AA, Romanos GE, Taniguchi Y, Sasaki KM, Zeredo JL, Koshy G, Coluzzi DJ, White JM, Abiko Y, Ishikawa I, Izumi Y. Periodontal and peri-implant wound healing following laser therapy. Periodontol 2000. 2015 Jun;68(1):217-69. doi: 10.1111/prd.12080.
Results Reference
result
PubMed Identifier
30422756
Citation
Shibli JA. Is Laser the Best Choice for the Treatment of Peri-Implantitis? Photomed Laser Surg. 2018 Nov;36(11):569-570. doi: 10.1089/pho.2018.4521. No abstract available.
Results Reference
result
PubMed Identifier
25494600
Citation
Feres M, Figueiredo LC, Soares GM, Faveri M. Systemic antibiotics in the treatment of periodontitis. Periodontol 2000. 2015 Feb;67(1):131-86. doi: 10.1111/prd.12075.
Results Reference
result
PubMed Identifier
32844406
Citation
Feres M, Retamal-Valdes B, Fermiano D, Faveri M, Figueiredo LC, Mayer MPA, Lee JJ, Bittinger K, Teles F. Microbiome changes in young periodontitis patients treated with adjunctive metronidazole and amoxicillin. J Periodontol. 2021 Apr;92(4):467-478. doi: 10.1002/JPER.20-0128. Epub 2020 Oct 12.
Results Reference
result
PubMed Identifier
31994207
Citation
Teughels W, Feres M, Oud V, Martin C, Matesanz P, Herrera D. Adjunctive effect of systemic antimicrobials in periodontitis therapy: A systematic review and meta-analysis. J Clin Periodontol. 2020 Jul;47 Suppl 22:257-281. doi: 10.1111/jcpe.13264.
Results Reference
result
PubMed Identifier
31576959
Citation
Shibli JA, Ferrari DS, Siroma RS, Figueiredo LC, Faveri M, Feres M. Microbiological and clinical effects of adjunctive systemic metronidazole and amoxicillin in the non-surgical treatment of peri-implantitis: 1 year follow-up. Braz Oral Res. 2019 Sep 30;33(suppl 1):e080. doi: 10.1590/1807-3107bor-2019.vol33.0080. eCollection 2019.
Results Reference
result
PubMed Identifier
27013640
Citation
Tamashiro NS, Duarte PM, Miranda TS, Maciel SS, Figueiredo LC, Faveri M, Feres M. Amoxicillin Plus Metronidazole Therapy for Patients with Periodontitis and Type 2 Diabetes: A 2-year Randomized Controlled Trial. J Dent Res. 2016 Jul;95(7):829-36. doi: 10.1177/0022034516639274. Epub 2016 Mar 24.
Results Reference
result
PubMed Identifier
28303587
Citation
Borges I, Faveri M, Figueiredo LC, Duarte PM, Retamal-Valdes B, Montenegro SCL, Feres M. Different antibiotic protocols in the treatment of severe chronic periodontitis: A 1-year randomized trial. J Clin Periodontol. 2017 Aug;44(8):822-832. doi: 10.1111/jcpe.12721. Epub 2017 Jul 26.
Results Reference
result
PubMed Identifier
26285807
Citation
Carcuac O, Derks J, Charalampakis G, Abrahamsson I, Wennstrom J, Berglundh T. Adjunctive Systemic and Local Antimicrobial Therapy in the Surgical Treatment of Peri-implantitis: A Randomized Controlled Clinical Trial. J Dent Res. 2016 Jan;95(1):50-7. doi: 10.1177/0022034515601961. Epub 2015 Aug 18.
Results Reference
result

Learn more about this trial

Surgical Access Combined With Systematically Administered Antibiotics in the Treatment of Peri-implantitis

We'll reach out to this number within 24 hrs