A clinical trial to study the effects of adding magnesium sulfate with local anesthetic injection on evaluating shooting tooth pain during and after the treatment.
Phase 3
Completed
- Registration Number
- CTRI/2018/01/011569
- Lead Sponsor
- SRM Dental College Ramapuram
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 42
Inclusion Criteria
1.Patients diagnosed with symptomatic irreversible pulpitis and symptomatic apical periodontitis in mandibular posterior teeth (premolar or molar) of moderate to severe intensity (AAE).
2.Age group between 20 â?? 60 years.
3.Immediate response to electric pulp testing.
4.Ability to understand the use of pain scales.
5.Patients satisfying American Society of Anesthesiologist (ASA) category I and II.
Exclusion Criteria
1.Had taken any medications within 8 hours before treatment.
2.Allergic to local anesthesia.
3.ASA category of III or greater.
4.Pregnancy and Nursing.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anesthetic Efficacy, post operative analgesia onset and duration of 2% Lidocaine with Magnesium Sulfate ( 75mg, 150mg)Timepoint: 1. Immediate complete anaesthesia without supplementary injections in 5 to 15 minutes. <br/ ><br>2.Duration of anesthesia from the onset upto 3 hours. <br/ ><br>3. Post operative analgesia upto 48 hours. <br/ ><br>
- Secondary Outcome Measures
Name Time Method Onset and duration of anaesthesiaTimepoint: 1. Onset of anaesthesia: Within 3-5 minutes <br/ ><br>2. Duration of anaesthesia: More than 1.5 hours.