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Comparison the effect of chlorhexidine solution and toothbrush in the prevention of oral lesions

The comparison between chlorhexidine solution and toothbrush in prevention of oral lesions in patients hospitalized in intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014012216309N1
Enrollment
30
Registered
2014-04-18
Start date
2013-11-15
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

Condition 1: Gingivitis. Condition 2: Other diseases of lip and oral mucosa. Condition 3: Diseases of tongue. Gingivitis and periodontal diseases Other diseases of lip and oral mucosa Diseases of tongue

Interventions

Intervention 1: Intervention group: After approving of the study by sciences vice chancellor of Sabzevar University of medical sciences and completing the written consent forms by all participants i
Prevention
Intervention group: After approving of the study by sciences vice chancellor of Sabzevar University of medical sciences and completing the written consent forms by all participants in the study, Pat
Control group: control group members wash their mouth with 0.2 %( zero point two percent) chlorhexidine solution. This action is also done every 8 hours for 2 minutes during 4 days but for control

Sponsors

Vice-chancellor for Research of Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria: Having oral endotracheal tube, being 18-65 years old ,The absence of wound, infection and oral trauma, Not having diseases like hepatitis B and HIV; Not having any symptoms or antecedent of aspiration, serious problems, and artificial teeth. Exclusion criteria are: death at the time of the study, Separation from mechanical ventilation at the time of the study; View apparent aspiration, existence of allergic reactions; restrictions on procedures and aspiration risk.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Oral health. Timepoint: Daily for 4 days. Method of measurement: Beck Oral Assessment Scale and Mucosal Plaque Score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Alinejad Moghadam

Sabzevar University of Medical Sciences

mohammadalinegad23@yahoo.com+98 57 1441 9573

Outcome results

None listed

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