The effect of Persica and Protact herbal mouthwashes on the wound of gum surgery
Not Applicable
Recruiting
- Conditions
- Clinical dental crown lengthening surgery.
- Registration Number
- IRCT20170502033770N2
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 33
Inclusion Criteria
Patients should be between 18 and 60.
Patients with indications for clinical crown lengthening surgery on at least one tooth.
Patients agree to participate in the study.
Exclusion Criteria
They have used antibiotics for 10 consecutive days in the past 3 months.
They are allergic to mouthwash.
Patients have diabetes or any other systemic disease.
Patients take medications that interfere with gum healing, such as contraceptives.
They use corticosteroids.
They are pregnant or breastfeeding.
They use cigarettes.
They have pathological lesions in the oral mucosa.
They have removable dental prostheses or orthodontics.
They have periodontitis in the surgical area.
The teeth are discolored due to systemic factors or drugs.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Gingival index (GI). Timepoint: Measurement of gingival index on the day of surgery and 14 days after surgery. Method of measurement: by periodontal probe.;Plaque index (PI). Timepoint: Measurement of plaque index on the day of surgery and 14 days after surgery. Method of measurement: by dental explorer.
- Secondary Outcome Measures
Name Time Method Stain index (SI). Timepoint: 14 days after surgery. Method of measurement: by periodontal probe.;Changing the color of the tongue. Timepoint: 14 days after surgery. Method of measurement: observation.;Taste of the mouthwash. Timepoint: 14 days after surgery. Method of measurement: questionnaire.