Crown Lengthening.
Conditions
Interventions
Intervention 1: Control group: suture- in half of the patients silk 0.4 suture is placed and followed for two weeks. Intervention 2: Intervention group: tissue adhesive- in half of the patients PeriAc
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Patients who are candidates for crown lengthening surgery in maxillary premolars
Exclusion criteria
Exclusion criteria: Smoker patients Patient with any past history of systemic disease or sensitivity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAzarnoush Aryankia
Ahvaz University of Medical Sciences
Outcome results
None listed