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Clinical trial

Evaluation of anesthetic solution temperature effect on success of pulpal anesthesia following inferior alveolar nerve block injection in teeth with symptomatic irreversible pulpitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201109049322N1
Enrollment
60
Registered
2020-12-18
Start date
2020-11-16
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Inferior alveolar nerve block anesthesia.

Interventions

Intervention 1: Intervention group: Anesthesia injection at a temperature of 37 ° C. Intervention 2: Intervention group: Anesthesia injection at a temperature of 4 ° C. Intervention 3: Control group:

Sponsors

Bojnourd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Presence a mandibular molar with symptomatic irreversible pulpitis Adults over 18 years old Patient permission

Exclusion criteria

Exclusion criteria: Patients who are alcohol or drug addicted or smoking Patients who are taking psychiatric drugs Patients who have a systemic disease affecting the dental treatment plan Patients who are taking painkillers on the day of injection Teeth which have calcification in the pulp and canal of the desired tooth Patients with history of dentoalveolar trauma Patients who do not have any symptom of lip numbness after a single inferior nerve block injection

Design outcomes

Primary

MeasureTime frame
Response to the electrical test. Timepoint: Before anesthesia injection - 15 minutes after anesthesia injection - 1 minute after the last test. Method of measurement: via electrical pulp tester.;Response to the cold test. Timepoint: Before anesthesia injection - 15 minutes after anesthesia injection - 1 minute after the last test. Method of measurement: Based on the standard cold test method for dental vitality testing.;Response to the Verbal Analog Scale. Timepoint: When preparing the access cavity. Method of measurement: Based on the patient's verbal response.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Dastpak

Bojnourd University of Medical Sciences

mahsa.dastpak@yahoo.com+98 58 3229 6764

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026