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Effect of subgingival irrigation with Chamomile on periodontal disease

Evaluation of the clinical effect of subgingival irrigation with chamomile, Persica and chlorhexidine on periodontal disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200215046505N1
Enrollment
11
Registered
2020-04-09
Start date
2015-12-22
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

periodontitis. Periodontal disease, unspecified

Interventions

Intervention 1: Intervention group:Immediately after scaling, each quadrant went under one of the subgingival irrigation with one of the mentioned materials, randomly. First groups material was Chammo

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with moderate to severe chronic periodontitis which has over 3 millimeters attachment loss Having at least 20 teeth Existence of at least a pocket depth of 5 millimeters or more in posterior teeth in each quadrant Slow rate of disease progression without familial aggregation Without any history of systemic disease Volunteers whom was referred to periodontology department of Shiraz school of dentistry

Exclusion criteria

Exclusion criteria: Any sub gingival crown or filling on the desired area History of allergy to chamomile Need for antibiotic prophylaxis History of any periodontal treatment and SRP in last 3 months Pregnancy Smokers Medical conditions which interfere with dental treatments

Design outcomes

Primary

MeasureTime frame
The rate of periodontal pocket depth. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: periodontal probe.;The rate of bleeding on probing. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: periodontal probe.;The rate of dental plaque. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: Disclosing agent.;Gingival recession rate. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: periodontal probe.;Mucogingival junction. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: periodontal probe.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Emami

Shiraz University of Medical Sciences

zahra_emami63@yahoo.com+98 71 3626 3193

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026