Periodontal flap surgery. Periodontal disease, unspecified
Conditions
Interventions
Intervention 1: Intervention group: After the surgery, we use the 20% Propolis gel, which is made by the Company that produces the Propolis (Green Plants of Life Company) under the Coe Pack( GC Americ
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with moderate to severe chronic Periodontitis require two side or whole mouth periodontal flap surgery that is systemically healthy The same type of flap on both sides in each person Age over 18 years Pelaque index = 1 after health education No contraindications for surgery No need to cut more than 2 mm of bone No need for prophylactic Antibiotics Do not take Corticosteroids or Hormones for the past two months Having acceptable cooperation
Exclusion criteria
Exclusion criteria: Smoking Pregnancy Taking anti-inflammatory drugs or Antibiotics Existence of systemic disease Pelaque index 2 or 3 after health education Need to cut more than 2 mm of bone Lack of cooperation and patient satisfaction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gingival healing index. Timepoint: One week after surgery, Two weeks after surgery, One month after surgery. Method of measurement: The healing rate is assessed based on tissue color, probe bleeding, granular tissue, cut margin, and discharge with five excellent, very good, good, weak, and very weak words. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pelaque index. Timepoint: Before surgery, One week after surgery, Two weeks after surgery and One month after surgery. Method of measurement: Based on the Silness and Loe method, it is evaluated in which the absence of Plaque(grade 0) to very large Plaque(grade 3) is ranked.;Papillary bleeding index. Timepoint: Before surgery, One week after surgery, Two weeks after surgery and One month after surgery. Method of measurement: It shows the rate of papillary bleeding by probe in 4 ranks, from non-bleeding (grade 0) to spontaneous bleeding (grade 3).;Pain index. Timepoint: Before surgery, One week after surgery, Two weeks after surgery and One month after surgery. Method of measurement: By the Visual Analog Scale form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSima Kiani
Esfahan University of Medical Sciences
Outcome results
None listed