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Comparison of the Clinical and Microbiological Effects of CHX and HOCl Containing Mouthwashes

B

Baskent University

Status

Completed

Conditions

Dental Plaque

Treatments

Other: HOCl
Other: CHX

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The primary objective of the study is to compare the antiplaque and anti-inflammatory effects of HOCl mouth rinse with those of CHX mouth rinse. The secondary objective is to evaluate and compare the antimicrobial activities of HOCl mouth rinse and CHX mouth rinse on dental biofilm.

Full description

The primary objective of the current clinical study is to compare the antiplaque and anti-inflammatory efficacy of HOCl mouth rinse with that of CHX mouth rinse. The secondary objective is to compare the antimicrobial activities of these two mouth rinses on dental biofilm. This single-center, triple-blind, randomized controlled crossover study was completed with 26 participants. In the study, the same participants used both HOCl (0.02%) and CHX (0.2%) mouth rinses over a 4-day re-plaque formation model. Following each mouth rinse usage, supragingival dental plaque biofilm samples were collected, and clinical parameters including the Modified Plaque Index, Bleeding on Probing Index, and Modified Stain Index were recorded. Additionally, participants were asked to evaluate the mouth rinses they used via a questionnaire. In conclusion, HOCl mouth rinse has demonstrated antiplaque efficacy comparable to that of CHX mouth rinse. When evaluating total bacterial counts, both mouth rinses exhibited similar antimicrobial effectiveness. Within the limitations of this study, HOCl may be considered a promising antimicrobial agent for dental plaque control.

Enrollment

26 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being systematically healthy
  • Having at least 22 natural teeth (236)
  • Not smoking
  • Participants must not drink alcohol and must work during their term

Exclusion criteria

  • Having periodontitis and gingivitis
  • Being breastfeeding or pregnant
  • Using medication that may affect periodontal status
  • Having used antibiotics in the last month
  • Having used any mouthwash in the last month
  • Using fixed, removable dentures or orthodontic appliances

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

26 participants in 2 patient groups

HOCl
Experimental group
Treatment:
Other: HOCl
CHX
Active Comparator group
Treatment:
Other: CHX

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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