The effect of premedication on tooth anesthesia

Phase 3

Recruiting

• Conditions: Irreversible pulpitis.

• Registration Number: IRCT20131216015814N3
• Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 March 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 88

Inclusion Criteria

Patients with first or second mandibular molars requiring root canal treatment with the diagnosis of symptomatic irreversible pulpitis and a history of spontaneous pain.
Patients who are completely healthy or have a mild systemic disease that is well controlled (ASA I, II)
Patients who have the ability to fill out a questionnaire and a consent letter
Patients over 18 years old

Exclusion Criteria

Patients with heart pacemakers
Asthma, coagulation disorders, immune deficiency, diabetes, hypertension, mental disorders
pregnancy
Sensitivity or contraindication for receiving lidocaine, articaine, epinephrine and NSAIDs
The presence of open apex or calcification in the root of the Intended tooth
The presence of extensive restoration or periodontal disease
use of analgesic drugs 12 hours before treatment

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain during cavity preparation. Timepoint: Fifteen minutes after injection. Method of measurement: Visual analogue scale.

Secondary Outcome Measures

Name	Time	Method
eed for complementary injection. Timepoint: Fifteen minutes after block injection. Method of measurement: Complementary anesthetizing.