Actively Recruiting
Comparison of Conventional Buccal Nerve Block Versus Buccal Nerve Trunk Block for Anaesthesia of Buccal Mucosa During Extraction of Mandibular Posterior Teeth
Led by Watim Medical & Dental College · Updated on 2026-02-04
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of two anesthesia techniques, conventional buccal nerve block and buccal nerve trunk block, for numbing the buccal mucosa during extraction of lower back teeth (mandibular molars). The study aims to compare these methods by measuring pain levels using a visual analogue scale and the need for additional anesthesia during the procedure. This randomized control trial is sponsored by Watim Medical & Dental College and focuses on adults aged 20 to 60 years undergoing dental extractions. Participants will receive anesthesia through one of two methods: the conventional buccal nerve block involves injecting 1 ml of lidocaine with epinephrine at the level of occlusion lateral to the last mandibular molar until bone contact is reached. The buccal nerve trunk block involves administering the same dose 10 mm above the occlusal plane lateral to the last mandibular molar. Both methods are procedures to numb the buccal mucosa to allow for pain-free tooth extraction. During the study, pain will be assessed both while giving the injection and during the tooth extraction using a visual analogue scale, where scores above 4 indicate significant pain. Researchers will also note if supplemental anesthesia injections are needed, defined as using more than one cartridge during the procedure. All evaluations will occur within two hours of anesthesia administration. Participants are monitored closely throughout the process to compare the pain perception and effectiveness of the two nerve block techniques.
CONDITIONS
Brief Title
Comparison of Conventional Buccal Nerve Block Versus Buccal Nerve Trunk Block During Extraction of Posterior Mandibular Teeth
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 20 to 60 years
- Patients of both genders
- Patients requiring extraction of mandibular molars
You will not qualify if you...
- Pregnant women
- Presence of cysts or tumors associated with teeth
- Patients receiving radiotherapy or chemotherapy
- Patients with mandibular fracture
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 2 hours after anesthesia administration
Participants receive anesthesia by either conventional buccal nerve block or buccal nerve trunk block during extraction of mandibular posterior teeth to assess pain perception and need for supplemental anesthesia.
1 procedure visit (in-person)
Trial Site Locations
Total: 1 location
1
Watim Medical College & Dental Hospital
Islamabad, Islamabad, Pakistan, Pakistan, 46500
Actively Recruiting
Research Team
S
Syed Saad Aftab Mohiuddin
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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