Effect of Sufentanil on the Rate of Anesthesia
Information source: Islamic Azad University, Tehran
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Irreversible Pulpitis
Intervention: Lidocaine with Epinephrine+ Normal saline (Drug); Lidocaine with Epinephrine + sufentanil (Drug)
Phase: Phase 2
Status: Completed
Sponsored by: Islamic Azad University, Tehran Official(s) and/or principal investigator(s):
Mandana Abedi Tari, Dentist, Principal Investigator, Affiliation: Dental School of Azad University
Summary
The aim of this study was to compare the effects of Lidocaine/epinephrine with and without
Sufentanil on the rate of anesthesia after supplemental intraligamentary injection (PDL) in
teeth with irreversible pulpitis.
Clinical Details
Official title: Comparison the Effect of Lidocaine (With Epinephrine) With and Without Sufentanil on the Rate of Anesthesia of Intra-ligamentary Injection in Teeth With Irreversible Pulpitis
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
Primary outcome: depth of anesthesia
Secondary outcome: intensity of the pain
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- patients in the age group of 18-65 years old
- healthy (ASA I, II)
- patients with first or second mandibular molars who need endodontic treatment
- vital tooth without a history of past endodontic treatment
- patients with clinical evidence of irreversible Pulpits with moderate to severe pain
- patients who signed consent form
- patients numbness at the lateral edge of the lips after inferior alveolar injection
(INA) and those with positive respond to maximum output of pulp tester after INA.
Exclusion Criteria:
- pregnant or nursing
- necrotic tooth
- patients with allergy or contraindication toward non-opioid or opioid painkillers
such as aspirin or NSAIDs
- Patients who have taken opioid or non opioid or steroid pain killers, antidepressants
or sedative drugs in the past 48 hours
- patient with infectious diseases
- patient with moderate to sever periodontal disease
- those without numbness at the lateral edge of the lips after inferior alveolar
injection (INA), and those do not respond to maximum output of pulp tester after
INA.
Locations and Contacts
Dental School of Azad University, Tehran, Iran, Islamic Republic of
Additional Information
Starting date: January 2010
Last updated: April 4, 2012
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