Evaluation of different wound closer methode in periodontal surgery
Not Applicable
- Conditions
- Crown Lengthening.
- Registration Number
- IRCT20190509043541N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Patients who are candidates for crown lengthening surgery in maxillary premolars
Exclusion Criteria
Smoker patients
Patient with any past history of systemic disease or sensitivity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative bleeding. Timepoint: 3 day after surgery. Method of measurement: On the third day, with the observation and clinical examination of the patient, the rate of postoperative bleeding (divided into: 1 - high bleeding 2 - low and continuous bleeding 3 - low bleeding and accidental bleeding 4 - bleeding 5 - no bleeding) (10) And are recorded on the respective charts.
- Secondary Outcome Measures
Name Time Method Wound healing index. Timepoint: 14 days after surgery. Method of measurement: wound healing index by observation and examination Clinical patient (including very weak, weak, satisfactory, good, very good).;Presence or non-sensitivity. Timepoint: 14 days after surgery. Method of measurement: sensitivity to the patient's clinical examination (including sensitization or not).;Lower bone matching. Timepoint: 14 days after surgery. Method of measurement: tissue fitting with the lower bone by observation and clinical examination of the patient (including Adapted and not compliant.;Pain score. Timepoint: 14 days after surgery. Method of measurement: the degree of pain was measured by asking the patient based on the use of VAS (visual scale) scaling from zero to ten (0 = painless to 10 = the worst pain possible).