Status:
COMPLETED
Ultrasonic vs Rotary Instruments in Impacted Mandibular Third Molar Surgery: Clinical and Salivary CRP Outcomes
Lead Sponsor:
Le Huynh Thien An
Conditions:
Impacted Mandibular Third Molar
Pain
Eligibility:
All Genders
18-35 years
Phase:
NA
Brief Summary
In the surgical removal of impacted mandibular third molars, ultrasonic surgical devices (piezosurgery) have been introduced with the expectation of reducing postoperative complications such as swelli...
Eligibility Criteria
Inclusion
- Healthy patients (ASA Physical Status index ≤ 2), aged 18-35 years.
- Patients presenting with bilateral impacted mandibular third molars of comparable difficulty, with the angulation difference between the two teeth not exceeding 15 degrees, as assessed according to the Pell and Gregory classification on panoramic radiographs.
- Patients who agree to participate in the study after being fully informed about the objectives and requirements.
Exclusion
- Patients with acute systemic or oral infection at the surgical sites.
- Patients with clinical evidence of tumors or cystic lesions, or radiolucent lesions larger than 3 mm on radiographs at the mandibular third molar site.
- Patients with a history of antibiotic or anti-inflammatory drug use within 3 weeks prior to study participation.
- Patients with psychiatric disorders, motor dysfunction, or trauma in the maxillofacial region.
- Patients with systemic diseases or medication use that reduces salivary secretion, such as Sjögren's syndrome or prior head and neck radiotherapy.
- Pregnant or breastfeeding women.
Key Trial Info
Start Date :
September 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 31 2025
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT07196904
Start Date
September 1 2024
End Date
August 31 2025
Last Update
October 1 2025
Active Locations (1)
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1
University of Medicine and Pharmacy at Ho Chi Minh City, Faculty of Dentistry
Ho Chi Minh City, Vietnam, 700000