Anesthetic Efficacy of X-tip Intraosseous Injection

Mashhad University of Medical Sciences40 enrolled

Overview

* Hypothesis: * X-tip intraosseous is an effective supplementary injection in mandibular hot teeth as well as Periodontal Ligament (PDL) injection * Purposes: * Comparing the anesthetic efficacy of X-tip intraosseous and PDL injection in mandibular hot teeth which had not been anesthetized after 3.6 ml Infra Alveolar Nerve Block * Methods and Materials: * forty patients with mandibular hot molar or second premolar which had not been anesthetized after 3.6 ml inferior alveolar nerve block injection will be selected for this study

* Randomization: * All patients will be randomly divided into two groups as follows: 1. X-tip intraosseous injection will be used as supplementary 2. PDL injection will be used as supplementary * Anesthetic evaluation: * For anesthetic evaluation we will use Visual Analog Scale (VAS)

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Masking

SINGLE

Enrollment

Conditions

Anesthesia

Interventions

Type of Supplementary InjectionPROCEDURE

Patients will be selected from a group who were not anesthetized following 3.6 ml block injection. Half of the randomly selected patients will receive X-tip intraosseous injection and half will receive PDL injection as a supplementary for completing the anesthesia in selected hot mandibular molar teeth.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 50 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Mandibular Molars and second premolars with Acute Irreversible Pulpitis * None of the teeth selected should have been anesthetized following 3.6 ml Lidocaine block injection Exclusion Criteria: * Unhealthy patients * Teeth which were anesthetized following 3.6 ml nerve block injection * Patients who did not have any signs of lip anesthesia following 3.6 ml injection

Locations (1)

Faculty of Dentistry

Mashhad, Khorasan Razavi, Iran

RECRUITING

Outcomes

Primary Outcomes

Number of participant who will have the pain following X-tip or PDL as a supplementary injection

All particiapant will be asked to show their pain degree on VAS for evaluation the efficacy of injections as a supplementary for anesthetising the teeth before and after the supplementary injection.

Time frame: 6 months

Secondary Outcomes

Heart rate monitoring

This record will be monitored by puls oximeter device

Time frame: before block injection and after supplementary injection

Central Contacts

Mina Zarei Binabaj, DDS,MSc

CONTACT

00985118829525 zareim@mums.ac.ir

Data from ClinicalTrials.gov

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