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Comparison of General Vi-one mouthwash with Chlorhexidine 0.2 %

Comparison of General Vi-one mouthwash with Chlorhexidine 0.2 % on periodontal parameters in patients with chronic periodontitis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015092724232N1
Enrollment
180
Registered
2015-10-22
Start date
2015-01-25
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic periodontitis. Periodontal disease, unspecified

Interventions

Intervention 1: In the intervention group after scaling and Brvsazh and health education, mouthwash is determined to use it twice a day for four weeks. Intervention 2: In the control group after scali
Prevention
In the intervention group after scaling and Brvsazh and health education, mouthwash is determined to use it twice a day for four weeks
In the control group after scaling and Brvsazh and health education, mouthwash is determined to use it twice a day for four weeks
After scaling and Brvsazh and health education control group, placebo-controlled study is to use it twice a day for four weeks

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ensuring the chronicity; there are pockets of 3-6 mm; absence of systemic diseases and pregnancy; lack of prior therapy or surgery in the absence of smoking; alcohol and antibiotics and drugs interfering with oral protests in the past 6 months and ultimately ensure patient cooperation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Probing Pocket Dept. Timepoint: Before and four weeks after intervention. Method of measurement: mm with the probe.;Clinical Attachment Level. Timepoint: Before and four weeks after intervention. Method of measurement: mm with the probe.;Bleeding Index. Timepoint: Before the experiment, four weeks after the intervention. Method of measurement: The percentage of points.;Plaque Index. Timepoint: Before the experiment, four weeks after the intervention. Method of measurement: Percent of levels.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahab Shahhosseini

Yazd University of Medical Sciences

shahabkorg.8870@yahoo.com+98 35 3724 9333

Outcome results

None listed

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