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Effect of sufentanil on the severe of anesthesia

Comparison of anesthetic efficacy lidocain / epinephrine with and without sufentanil for intra ligamentary injection in the mandibular posterior tooth with irreversible pulpitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110137790N1
Enrollment
60
Registered
2012-01-25
Start date
2010-10-14
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

irreversible pulpitis. Pulpitis

Interventions

Intervention 1: second group:0/4 ml lidocain with epinephrine and0/4 ml sufentanil ( 0/04 µg). Intervention 2: first group:0/4 ml lidocain %2 with epinephrine,0/4 ml salin.
Treatment - Drugs
second group:0/4 ml lidocain with epinephrine and0/4 ml sufentanil ( 0/04 µg)
first group:0/4 ml lidocain %2 with epinephrine,0/4 ml salin

Sponsors

Islamic Azad dental university of Tehran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with VITAL mandibular molars; patients with dental with irreversible pulpits clinical evidence; those candidates who suffer from moderate to severe pain; patients who signed consent form; those who felt with lip edge anesthesia after injection of infra alveolar (INA) and those who responded positively to output maximum of pulp tester. Exclusion criteria: Systemic disease; pregnancy and lactation; age: Patients under the age of 18 years and older than 65 years; infectious diseases; moderate to advanced periodontal disease; necrotic teeth; sensitivity OPIOIDs, Benzodiazepines, Barbiturate or use of them in the past 48 hours; those without lip edge anesthesia after injection of infra alveolar (INA), and those, does not respond to maximum output pulp tester after injection of INA.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of the pain. Timepoint: before intervention,during the intervention,in the immediately after injection,access cavity,initial file,pulpotomy,pulpectomy. Method of measurement: with visual analogue scale(VAS).;Depth of anesthesia. Timepoint: before intervention,during the intervention,in the 1,5,9,13,17th minuths. Method of measurement: with electric pulp tester.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Peyman Mehrvarz far

Islamic Azad dental university of Tehran

?peymanm@dentliau.ac.ir+98 21 2256 4571

Outcome results

None listed

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