Warm Versus Conventional 2% Lignocaine for IANB Efficacy
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-50
SponsorArmed Forces Institute of Dentistry, Pakistan
About this trial
The study compares the anesthetic efficacy of warm versus conventional 2% lignocaine for inferior alveolar nerve block in mandibular molars, evaluating success rates and onset time.
Eligibility criteria
Qualifiers
Permanent teeth with acutely inflamed pulp without swelling or draining sinus.
Patient who have carious mandibular molars.
Patients of either gender aged between 18-50 years old.
Systemically healthy patients.
Disqualifiers
Patients on preoperative analgesics and antibiotics.
Teeth with calcified canals and previously treated teeth.
Pregnant and lactating mothers.
Patients who are immunocompromised, anxious and mentally handicapped.
Trial design
Treatments tested in this trial
- conventional 2% lignocaine at room temperature
- pre-warmed 2% lignocaine at 42°C
Treatment groups
200 Participants
are divided into 2 treatment groupsLocations
1Armed Forces Institute Of Dentistry46000, RawalpindiPunjab Province, Pakistan
Sponsors and collaborators
Armed Forces Institute of Dentistry, Pakistan
Lead sponsor
Source ClinicalTrials.gov