None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients classified as ASA I (systemically healthy) Patients aged 18 35 years Patients requiring surgical removal of bilateral impacted mandibular third molars Patients willing to participate in the study and provide written informed consent
Exclusion criteria
Exclusion criteria: Patients with systemic diseases (diabetes, immunocompromised status, bleeding disorders) Pregnant or lactating females Smokers and tobacco users Patients with a history of radiation therapy or organ transplantation Patients allergic to local anaesthetic agents Patients who have taken antibiotics, anti-inflammatory or antimicrobial drugs within 7 days prior to surgery Patients with acute local infection at the surgical site
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduced postoperative pain Reduced facial swelling Reduced trismus Better wound healing Lower incidence of dry socket and postoperative infection Improved patient comfort and recovery compared to normal saline irrigationTimepoint: 1,3,7 days | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Kalinga Institute of Dental Sciences