The Effect of Probiotic Supplementation in the form of Mouthwash with Scaling and Root planing on the Periodontal Indeces in Patients with Generalized Chronic Periodontitis

Clinical trial The Effect of Probiotic Supplementation in the form of Mouthwash with Scaling and Root planing on the Periodontal Indeces in Patients with Generalized Chronic Periodontitis

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180630040290N2

Enrollment

Registered

2019-03-27

Start date

2019-03-01

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

The effect of probiotic supplementation in the form of mouthwash with scaling and root planing on the periodontal indeces in patients with generalized chronic periodontitis.

Interventions

Intervention 1: Intervention group: The intervention group after SRP will use probiotic for 20 days by daily solution of two probiotic capsules in 250 cc water and then will gargle in the mouth for 30

Eligibility

Sex/Gender

All

Age

29 Years to 59 Years

Inclusion criteria

Inclusion criteria: Patients suffering chronic generalized periodontitis with clinical attachment loss (CAL)=4 millimeters who are systemically healthy.

Exclusion criteria

Exclusion criteria: Patients with any systemic disease, that could affect periodontium disease Sensitivity to probiotic supplements Antibiotic therapies in the last 3 months Pregnant and lactating women Allergic patients to lactate products Patients with inappropriate collaboration (High level of plaque index in the periodic examinations)

Design outcomes

Primary

Measure	Time frame
Clinical attachment level (CAL). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: measurement of the distance between the stent margin to the sulcus base by means of a periodontal probe.;Plaque index (Pl). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: By disclosing agent with visual scale.;Bleeding on probing (BOP). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: Bleeding in 15 seconds after gentle probing by periodontal probe.;Probing depth (PD). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: The distance between the mucosal margin and the sulcus base by periodontal probe in millimeters.	—

Measure

Time frame

Clinical attachment level (CAL). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: measurement of the distance between the stent margin to the sulcus base by means of a periodontal probe.;Plaque index (Pl). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: By disclosing agent with visual scale.;Bleeding on probing (BOP). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: Bleeding in 15 seconds after gentle probing by periodontal probe.;Probing depth (PD). Timepoint: Before the intervention , one months after initiating the intervention and three months after initiating the intervention. Method of measurement: The distance between the mucosal margin and the sulcus base by periodontal probe in millimeters.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirreza Babaloo

Tabriz University of Medical Sciences

Amirrezababaloo@yahoo.com+98 41 3335 5921

Outcome results

None listed

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