Evaluation the effect of non-eugenol periodontal dressing (Coe-Pak) on pain and wound healing after crown lengthening surgery.
Conditions
Interventions
Intervention group: In the intervention group, after performing crown lengthening surgery and suturing, we apply periodontal Coe-Pak dressing according to the manufacturer’s instructions and in an ade
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age 18 years and older Ability to respond to the questionnaire items Informed consent to participate in the study Absence of systemic disease No contraindications for surgery Need for functional crown-lengthening surgery in only one tooth
Exclusion criteria
Exclusion criteria: Lack of willingness to continue cooperation during the study Failure to attend postoperative follow-up visits Improper completion of the forms Partial or complete loss of the periodontal dressing before the first follow-up appointment (7 days after surgery) Allergic reaction to the periodontal dressing Occurrence of pulpal changes after the surgical procedure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Our primary outcome variable is pain assessment using the Visual Analog Scale (VAS). We will compare pain levels between individuals who receive a periodontal pack (Co-Pac) after crown-lengthening surgery and those who do no. Timepoint: Pain will be measured during the first 7 days following the crown-lengthening procedure. Method of measurement: pain will be measured using the Vas scales (0-10). | — |
Secondary
| Measure | Time frame |
|---|---|
| Presence of infection after surgery. Timepoint: One week after the operation. Method of measurement: Infection is evaluated based on the presence of swelling, redness, and pain. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPouria Batoei
Mashhad University of Medical Sciences
Outcome results
None listed