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Control of Periodontal Infections

Control of Periodontal Infections

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01098448
Enrollment
187
Registered
2010-04-02
Start date
1999-09-30
Completion date
2004-12-31
Last updated
2010-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontitis

Keywords

Amoxicillin, antibiotics, chronic periodontitis, local drug delivery, metronidazol, randomized controlled trial, subgingival scaling, surgery, tetracycline, moderate to advanced chronic periodontitis

Brief summary

The purpose of this study is to test combined effects of scaling and root planing with periodontal surgery, systemically administered amoxicillin and metronidazole, and/or local tetracycline on pocket depth reduction and attachment level gain in patients with chronic periodontitis.

Detailed description

In this 2x2x2 factorial design study, 229 moderate to advanced chronic periodontitis patients stratified according to current smoking status were recruited in USA and Sweden. Patients were randomly assigned to 8 groups, all of which were treated by SRP plus none, one, two or three adjunctive treatments. Thus, patients were assigned to groups that did or did not receive Surg, LAb, SAb or LAb+SAb (All) providing 8 treatment combinations (Surg + All, Surg + SAb, Surg + LAb, Surg alone, SRP + All, SRP + SAb, SRP + LAb, SRP alone). Clinical, microbiological and immunological measurements were taken for 2 years (at baseline, 3, 6, 12, 18 and 24 months). To focus on changes diseased sites, analysis was restricted to sites with baseline pocket depth greater than 5 mm. (also, these were the only sites treated by LAb). In this report, main effects and interactions were evaluated for PD reduction and AL gain two years post therapy for 187 of patients. Mean values were computed for each treatment group and averages after 2 years were compared to baseline by ANOVA. Factorial ANCOVA was used to examine significance of differences between Surg or not, SAb or not and LAb or not for PD reduction and AL gain using baseline attachment level or pocket depth as covariates and including current smoking as a factor.

Interventions

OTHERscaling and root planing

scaling and root planing as a single therapy

DRUGlocal tetracycline

local delivery of tetracycline fibers releasing approximately 1.7 mg/tooth in all pockets \>5mm

DRUGsystemic metronidazole and amoxicillin

systemic metronidazole (250 mg tid x 14) and amoxicillin (500 mg bid x 14

OTHERsurgery

periodontal surgery in residual pockets of \>4mm

DRUGlocal antibiotics and systemic metronidazole and amoxicillin

1.7 mg/tooth tetracycline fiber plus metronidazole (250 mg tid x14d)and amoxicillin (500 mg bid x 14d)

OTHERlocal tetracycline and periodontal surgery

local delivery of tetracycline fibers releasing approximately 1.7 mg/tooth in all pockets \>5mm and periodontal surgery in residual pockets of \>4mm

OTHERperiodontal surgery and systemic metronidazole and amoxicillin

surgery in residual pockets \>4mm and metronidazole (250mg tidx14d) and amoxicillin (500mg bidx14d)

OTHERsurgery, local tetracycline, systemic metronidazole and amoxicillin

periodontal surgery in residual pockets \>4mm, tetracycline ibers releasing approximately 1.7 mg/tooth in pockets \>5mm, systemic metronidazlo (250mg tidx14d) and amoxicillin (500 mg bidx14d)

Sponsors

Göteborg University
CollaboratorOTHER
Boston University
CollaboratorOTHER
The Forsyth Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* greater than 20 years of age * had a least 15 natural teeth * in good general health * at least 4 teeth with pockets \> 6 mm * at least 8 teeth with AL \> 3 mm at baseline

Exclusion criteria

* pregnant or nursing (if female) * having antibiotic or periodontal therapy in the previous three months * systemic conditions that would affect the course of periodontal disease * systemic conditions that required antibiotic coverage * allergic to drugs used in the study

Design outcomes

Primary

MeasureTime frame
Clinical Attachment Level Gain24 months

Secondary

MeasureTime frame
Probing pocket depth reduction24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026