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Clarithromycin is an Adjunct to Scaling and Root Planing

Efficacy of Clarithromycin is an Adjunct to Scaling and Root Planing .A Clinical Microbiological and Immunological Study.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02359721
Acronym
CASRCMI
Enrollment
30
Registered
2015-02-10
Start date
2012-01-31
Completion date
2013-12-31
Last updated
2015-02-10

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

Conditions

Periodontitis

Keywords

Colony forming units Antimicrobial agents, Microbial colonization

Brief summary

The present study was done to evaluate the effect of clarithromycin as an adjunct to scaling and root planning at baseline, three months and six months intervals . Clinical, microbiological and immunological parameters were taken. Clinical parameters include gingival index , probing depth and clinical attachment level. In the present study, improved clinical and microbiological outcomes were attained using adjunctive clarithromycin, including GI, PD reduction, CAL gain and reductions in the frequency of detection of C-reactive protein, Pg, Aa. These results together with the recommended easy dosage and limited side effects make the use of this antibiotic in the treatment of periodontitis patients but only for a shorter period of time.

Detailed description

Background & Objectives: Along with conventional non-surgical periodontal therapy (NSPT) systemic antimicrobials may provide more effective treatment for chronic periodontitis by targeting tissue-invasive bacteria. The aim of this study was to evaluate the adjunctive effects of oral clarithromycin (CLM) to nonsurgical periodontal therapy for chronic periodontitis. Materials and Methods: 30 patients were categorized into two groups: test group - Base line scaling and root planing(SRP) was done. Clarithromycin tablet 500 mg( Clarino-500) was given for a period of 7 days orally two times per day. control group -only SRP done . Clinical parameters were recorded at baseline , 3 months, and six months interval .They included gingival index (GI), probing depth (PD), and clinical attachment level (CAL). Also microbial analysis of subgingival plaque samples was done at baseline, 3months and six months interval to estimate the levels of Pg and Aa bacteria using culture methods. Immunological parameter like estimation of C-Reactive protein was done in both groups at baseline 3 months and 6 months period. tests were used for statistical analysis.

Interventions

DRUGtablet clarithromycin 500 mg (Clarino-500) orally

orally

Sponsors

Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients age ranged between 30- 50 years with chronic periodontitis * Patients with Probing Depth (PD)- \>5mm, Clinical Attachment Level( CAL)- \>3mm * Systemically healthy individuals

Exclusion criteria

* Patients below the age of 30 years * Patients who have undergone periodontal therapy 3 months prior to study * Active /passive smokers * Any antibiotic use 3 months prior to study * Pregnant women and lactating mothers * Un co- operative/ retarded patients * Drug allergy/ other allergies * Any systemic diseases

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of Clarithromycin, as measured by reduction Gingival bleeding6 months0,3,6 months
Efficacy of Clarithromycin, as measured by Pocket probing depth6 months
Efficacy of Clarithromycin, as measured by Clinical attachment gain6 months
c-reactive protein levels6 months
Pg and Aa bacterial count6 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026