Evaluating the effect of conventional local anaesthesia anaesthesia (lignocaine), warming it and adding a buffer on the success of a nerve block in lower primary posterior teeth
Phase 2
Completed
- Conditions
- Health Condition 1: null- children aged 6-12 years, with bilateral vital pulp involvement in primary mandibular molars.
- Registration Number
- CTRI/2017/02/007922
- Lead Sponsor
- Reenu Sarah Kurien
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1.patients having deep dentinal caries extending through half the dentinal depth wrt 74, 75, 84, 85
2. patients complaining of mild to moderate pain.
3.teeth with vital pulp
4.children with frankl behaviour rating of 3 or 4
5.patients whose parents/guardians give consent
6.subjects should be free of systemic disease
7.the agreement to comply with study visits and procedures.
Exclusion Criteria
1.patients who are physically or medically compromised/ systemic disease
2.patients with allergies to local anaesthetics, sulphites or sodium bicarbonate
3.patients on any medication
4.presence of abscess or sinus openings at the site of injection or at the tooth involved.
5.children with frankl behaviour rating of 1 or 2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Anaesthetic efficacy <br/ ><br>2.The patientâ??s pain reactionTimepoint: 3-5 hours
- Secondary Outcome Measures
Name Time Method 1.Pain during administration of anaesthesia <br/ ><br>2.Onset of anaesthesia <br/ ><br>3.Pain while performing pulp therapy <br/ ><br>4.Duration of anaesthesiaTimepoint: 3-5 hours