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Analgesic Effects of Extraoral Ultrasound Block of Mandibular Nerve for the Extraction of Lower Third Molars

Analgesic Effects of Extraoral Ultrasound Block of Mandibular Nerve for the Extraction of Lower Third Molars

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06009302
Enrollment
36
Registered
2023-08-24
Start date
2023-09-01
Completion date
2023-12-31
Last updated
2024-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impacted Teeth, Molar

Keywords

dental anesthesia, inferior alveolar nerve, regional anesthesia, ultrasound, mandibular nerve

Brief summary

This is a study about the dynamics and effects of different types of blocks (intraoral conduction anesthesia of the alveolar nerve and extraoral US block of the mandibular nerve) for extraction of lower third molars.

Detailed description

Standard method of anesthesia for extraction of horizontally positioned lower thirdmolars is intraoral conduction anesthesia of the inferior alveolar nerve. However, the analgesiceffect of block is short and it is necessary to use analgesics. In this prospective clinical study,analgesic effect of ultrasound (US) -guided extraoral block of mandibular nerve will beinvestigated, in order to prolong pain-free time and reduce the use of analgesics associated withrisks (bleeding, hepatotoxicity). Characteristics of alveolar nerve block and US block of the mandibular nerve will becompared, such as: pain during application of anesthesia, amount of anesthetic, duration ofanesthesia, need to use analgesics, time to and level of pain when using analgesics, andcomplications

Interventions

PROCEDUREUS guided block of mandibular nerve

Extraoral ultrasound-guided block of the mandibular nerve will be performed in the examined group using an ultrasound device, using ropivacaine (0.75%, 2.5 mL).

PROCEDUREIntraoral block of lower alveolar nerve

Block of lower alveolar nerve will be applied intraoraly using articaine+adrenaline

Sponsors

Clinical Hospital Centre Zagreb
CollaboratorOTHER
Varazdin General Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* age 18-64 years * horizontally placed lower third molars * ASA I or II group

Exclusion criteria

* allergy to local anesthetics * local infection at the site of needle puncture * parotitis * serious liver disease * use of antiarrhythmics group III (eg amiodarone), anticoagulant or antithrombotic drugs * lactation * people who took an analgesic as a preventive measure before coming to the procedure

Design outcomes

Primary

MeasureTime frame
Time without painfirst 24 postoperative hours

Secondary

MeasureTime frameDescription
Time of numbnessfirst 24 postoperative hours
Pain level when anesthesia is appliedfirst 24 postoperative hours0-10 on VAS
Pain level when painkiller is neededfirst 24 postoperative hours0-10 on VAS

Countries

Croatia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026