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Comparison of the effectiveness of shallomin II and chlorhexidine mouthwashes in treating plaque induced gingivitis

Comparison of the effectiveness of shallomin II and chlorhexidine mouthwashes in treating plaque induced gingivitis: A clinical trial and microbiologic study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230305057627N1
Enrollment
36
Registered
2023-04-17
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

gingivitis. Chronic gingivitis, plaque induced

Interventions

Intervention 1: Intervention group: 18 patients should use Shallomin II mouthwash twice a day for 2 weeks, each time at 5 cc for 30 seconds, and avoid eating and drinking for 30 to 45 minutes. The pat

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Systemically healthy The presence of more than 20 permanent teeth (except the third molar) Untreated gingivitis (probing depth less than equal to 3, no clinical attachment loss, no evidence of radiographic bone loss.) The percentage of areas with bleeding during probing should be more than 30% Not using antibiotics and anti-inflammatory drugs in the last three months No mouthwash has been used in the past month Do not use cigarettes or alcohol Do not have mental retardation Not during pregnancy or breastfeeding

Exclusion criteria

Exclusion criteria: The presence of any pathology in the oral mucosa Acute gingivitis

Design outcomes

Primary

MeasureTime frame
Gingival Index (Sillness & loe). Timepoint: At the beginning of study, seventh day and fourteenth day. Method of measurement: Using a periodontal probe.;Plaque Index (Loe & Sillness). Timepoint: At the beginning of study, seventh day and fourteenth day. Method of measurement: Using a periodontal probe.;Total colony count. Timepoint: At the beginning of study, seventh day and fourteenth day. Method of measurement: Counting and recording.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Kaviani Nezhad

Ahvaz University of Medical Sciences

rezakv999@gmail.com+98 61 3376 5825

Outcome results

None listed

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