The effect of the propolis in oral wound healing
Phase 2
- Conditions
- -.-
- Registration Number
- IRCT2016102630475N2
- Lead Sponsor
- Vice chancellor for research, Dentistry faculty, Tehran University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
bone removal scale in their surgery was between 1-2 mm; their surgical time duration lasted between 90-115 minutes and had been used from both of chisels and bur in their surgery; don’t have any systematically problem; no periodontal disease in the surgical site; no restriction on surgery; don’t need to the antibiotic prophylaxis during the surgery; don’t use the corticosteroids or hormone in the last 2 months.
Exclusion criteria: when there is a problem in recording the patient’s information; smoking.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 0,1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Burning sensation. Timepoint: 0, 1,2,3,4,5,6 and 7 days after surgery. Method of measurement: Visual Analog Scale.;Consistency of gingiva. Timepoint: 7th day after surgery. Method of measurement: palpation with a blunt instrument.;Colour compatibility. Timepoint: 7th day after surgery. Method of measurement: Visual Analog Scale.;Infection. Timepoint: 2nd & 7th days after surgery. Method of measurement: Clinical examination.;Bleeding during probing. Timepoint: 7th day after surgery. Method of measurement: Probing.
- Secondary Outcome Measures
Name Time Method -. Timepoint: -. Method of measurement: -.