Pain after Crown Lengthening surgery. Acute pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Control group:At the end of the surgery, 20 milliliters of room temperature saline solution is used for irrigation for 5 minutes, after which the surgical site is sutured with 5-0 nylo
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Candidates for crown lengthening surgery of maxillary and mandibular molars Patients aged 18-60 years Clinical crown lengthening requires bone removal (osseous surgery). At least two adjacent teeth need to be present, with at least one being a molar. Patients must meet surgical criteria (ASA I, ASA II) and have no uncontrolled systemic diseases. Endodontically treated teeth must have documentation of future endodontic and prosthetic treatment.
Exclusion criteria
Exclusion criteria: Use of antidepressants or any medications that may affect the patient's perception of pain Use of NSAIDs due to systemic issue Pregnant women Use of tobacco Alcohol use Illicit drug use Concurrent use of antibiotics or analgesics during surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity based on VAS tool. Timepoint: Measurement of pain levels up to 24 hours post_surgery. Method of measurement: Visual Analogue Scale.;Number of analgesics consumed by the patients. Timepoint: 10 days post_surgery. Method of measurement: As reported by the patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| The time to first analgesic intake. Timepoint: Up to 24 hours post_surgery. Method of measurement: As reported by the patient.;Number of days experiencing pain. Timepoint: 7 days post_surgery. Method of measurement: As reported by the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Amini
Tehran University of Medical Sciences
Outcome results
None listed