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Randomized, Double blind clinical study alcohol free chlorhexidine with a cetylpyridinium chloride mouth rinses in periodontal diseases

A Comparison of mouth rinse containing alcohol free chlorhexidine with a cetylpyridinium chloride in periodontal diseases

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014051717587N6
Enrollment
24
Registered
2014-08-28
Start date
2014-07-10
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

Periodontal diseases. Periodontal diseases

Interventions

Intervention 1: Group A: perform daily mouthwashes twice a day with the solution containing 10 ml of 0.05 cetylpyridinium, (Vi-one, Rojin, Cosmetic-Lab, Kurdistan -Iran). Intervention 2: Group B: us
Treatment - Drugs
Group A: perform daily mouthwashes twice a day with the solution containing 10 ml of 0.05 cetylpyridinium, (Vi-one, Rojin, Cosmetic-Lab, Kurdistan -Iran).
Group B: use daily mouthwashes twice a day with 10ml of the non- alcoholic chlorhexidine (Kin Labratories, Spain).

Sponsors

Deputy of Research Council Of Dental Branch, Islamic Azad University of Tehran
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: adult patients, older than 18 years old, systemically healthy, and having at least 20 teeth. Exclusion criteria: patients with cavitated caries, no periodontal pockets larger than 4 mm, orthodontic appliances or removable prostheses, allergies to cetylpyridinium or CHX, use of antibiotics and anti-inflammatory drugs in the past 3 months that might alter normal gingival health, oral prophylaxis outside of study; use of oral chlorhexidine products or participation in an oral rinse study within 3 months prior to baseline examination, pregnancy or nursing, smoking.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction of pocket depth. Timepoint: One month. Method of measurement: Periodontal pobe.

Secondary

MeasureTime frame
Reduction of plaque index. Timepoint: One month. Method of measurement: Plaque Index (O’Leary).;Reduction of bleeding on probing. Timepoint: One month. Method of measurement: Bleeding index (Carterand Barnes).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Farahmand

Dental Branch, Islamic Azad University of Tehran

perio-implant@hotmail.com+98 21 2284 0604

Outcome results

None listed

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