gingival graft due to lack of attached gingiva.
Conditions
Interventions
Intervention 1: in control area, propolis-free oral ointment containing pectin, paraffin and carboxy methyl cellulose is applied over the palatal wound. Intervention 2: in the test area is protected b
Treatment - Drugs
in control area, propolis-free oral ointment containing pectin, paraffin and carboxy methyl cellulose is applied over the palatal wound
in the test area is protected by oral ointment containing 3.6 % propolis.
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: no systemic disease interfere with the wound healing, no cigarette smoking, no allergy to honey Exclusion criteria: patients without cooperation during the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain level. Timepoint: on 1st, 3rd, 7th, 14th and 21st days following the surgery. Method of measurement: visual analogue scale.;Dimensional changes. Timepoint: 7th, 14th, 21st , 30th, 42nd days. Method of measurement: Dimensional changes are evaluated via photographs which are taken at baseline and 7th, 14th, 21st , 30th, 42nd days from palatal wound area. Dimensional changes are evaluated with AutoCAD software and predetermined scale.;Thickness of palatal donor site. Timepoint: 0, 30th and 42nd days. Method of measurement: measured using a sterile kfile #15 on 4 sites of wound area at baseline and 30th, 42nd days and the mean value is recorded.;Color match. Timepoint: 7th, 14th, 21st , 30th, 42nd days. Method of measurement: Color coordination of donor site and adjacent normal tissues are evaluated using Photoshop software. | — |
Secondary
| Measure | Time frame |
|---|---|
| Burning sensation. Timepoint: on 1st, 3rd, 7th, 14th and 21st days. Method of measurement: by asking patients, yes or no.;Number of pain killers consumed. Timepoint: 21st day. Method of measurement: by asking patients.;Number of days patients take the pain killers. Timepoint: on 21st day. Method of measurement: by asking patient.;Bleeding of the wound. Timepoint: on 7th, 14th, and 21st days. Method of measurement: by rubbing the gauze on the wound/ yes or no. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarzaneh Dashkhaneh
Qazvin University of Medical Sciences
Outcome results
None listed