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Propolis In The Treatment Of Periodontitis

Propolis In The Treatment Of Chronic Periodontitis - A Clinicomicrobiologic Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01943877
Acronym
PROPOLIS
Enrollment
20
Registered
2013-09-17
Start date
2012-12-31
Completion date
2013-10-31
Last updated
2013-09-17

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

Conditions

Chronic Periodontitis

Brief summary

This study was conducted to evaluate by clinical and microbiological parameters the effect of locally delivered propolis as an adjunct to scaling and root planing in the treatment of chronic periodontitis.

Detailed description

Materials and Methods: 20 subjects diagnosed with chronic periodontitis were recruited to participate in split-mouth design and provided informed consent. Subgingival plaque sampling and clinical recording at baseline, 15 days and 1 month was performed. The patients received scaling and root planing, followed by Propolis administration subgingivally in the test sites. Significant differences between test and control were evaluated using the Mann-Whitney U test and Wilcoxon rank test.

Interventions

scaling root planing

DRUGPropolis

experimental

Sponsors

Rajarajeswari Dental College & Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* good general health * chronic periodontitis * minimum of 20 natural teeth with at least one pocket per quadrant * probing depth (PD) between 5 and 8 mm.

Exclusion criteria

* subgingival instrumentation within 3 months * antibiotic therapy within 3 months prior to the start of the study; * smokers * pregnant or nursing women * intolerance or allergy to honey products

Design outcomes

Primary

MeasureTime frame
Change in the probing pocket depth and clinical attachment levelthree time points of baseline,2 weeks, 4 weeks

Secondary

MeasureTime frame
change in gingival index and microbiological changesthree time points baseline, 2 weeks, 4 weeks.

Countries

India

Outcome results

None listed

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