Effectiveness of retromolar trigon injection as supplementary anesthesia in mandibular molar surgery

Not Applicable

Recruiting

• Conditions: The presence of anatomical variables of retromolar foramen and retromolar canal.

• Registration Number: IRCT20240205060911N1
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 26 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

Patients who are surgical candidates for extraction of mandibular molars
Identification of retromolar canal in panoramic or CBCT

Exclusion Criteria

Mandibular fracture
Surgical removal of the mandibular third molar
Mandibular orthognathic surgery
Pathological lesion or osteomyelitis in the mandibular ramus, angle and proximal part of the mandibular body
Osteoradionecrosis and history of radiotherapy
Central or peripheral pathological lesion removal in the mandibular ramus, angle or proximal part of the mandibular body
Medical disorders including neurovascular system and mental disorders
Surgery under anesthesia and sedation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain level during incision of mucoperiosteal flap in patients with retromolar injection and patients without retromolar injection. Timepoint: 5 minutes after the anesthesia intervention. Method of measurement: Visual Analogue Scale questionnaire.;Pain level when lifting the mucoperiosteal flap in patients with retromolar injection and patients without retromolar injection. Timepoint: 5 minutes after the anesthesia intervention. Method of measurement: Visual Analogue Scale questionnaire.;Pain level during osteotomy in patients with retromolar injection and patients without retromolar injection. Timepoint: 5 minutes after the anesthesia intervention. Method of measurement: Visual Analogue Scale questionnaire.;Pain level during tooth elevation in patients with retromolar injection and patients without retromolar injection. Timepoint: 5 minutes after the anesthesia intervention. Method of measurement: Visual Analogue Scale questionnaire.

Secondary Outcome Measures

Name	Time	Method
Observation of gentle and diffus hemorrhage from the socket during surgical intervention (oozing). Timepoint: After beginning of the intervention. Method of measurement: Observational.