Comparison of Conventional Buccal Nerve Block Versus Buccal Nerve Trunk Block During Extraction of Posterior Mandibular Teeth

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-60
SponsorWatim Medical & Dental College

About this trial

This randomised control trial will compare the efficacy of conventional buccal nerve block versus buccal trunk block using visual analogue scale to evaluate pain and additional anesthesia injection during extraction of mandibular molars.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 20 to 60 years

Patients of both gender

Patient requiring extraction of mandibular molars

Disqualifiers

Pregnant women

Pathologies associated with teeth i.e. cysts, tumors

Patients on radiotherapy or chemotherapy

Patients with mandibular fracture

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional Buccal Nerve Block

    Procedure/Surgery

    Arm Description: Administration of anesthesia at the level of occlusion lateral to last mandibular molar. Needle is inserted until bone contact is achieved. 1ml lidocaine with 1:100000 anesthesia is administered.

  • Buccal Nerve Trunk Block

    Procedure/Surgery

    Arm Description: Administration of anesthesia 10 mm above occlusal plane lateral to last mandibular molar. 1ml lidocaine with 1:100000 anesthesia is administered.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Conventional Buccal Nerve Block for anesthesia of buccal mucosaExperimental treatment 1 intervention
Group B: Buccal Nerve Trunk BlockExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Intraoperative pain perception

It was assessed while giving injection and during extraction of the tooth using the visual analog scale (VAS) scores. Facial pain scale uses facial expression to evaluate the amount of pain. It has scores ranging from 0 to 10 with 0 as the least pain and 10 as the worst pain. Score of more than 4 will be labelled as positive pain perception.

Time frame
Within 2hours of anesthesia administration
2

Need for supplemental infiltration

Use of more than 1 anesthesia cartridges during procedure will be labelled as need for supplemental infiltration.

Time frame
Within 2 hour of initial anesthesia administration

Secondary outcomes

Other outcomes

Sponsors and contacts

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