to check the pain perception of local anesthetics when the injection site is precooled with ice in patients requiring restorative or endodontic treatment of upper left and right molars.
Phase 1
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/067040
- Lead Sponsor
- DR F RIZWAN AHMED
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with good health in the age group of 18-50 years.
2.Patients scheduled to receive treatment of maxillary first and second molars for either Restorative or Endodontic treatment.
3.Patients with preoperative pain score 0-85mm as measured on HP-VAS scale.
Exclusion Criteria
Individuals with systemic and mental illness.
Individuals with known allergy or contraindication to lignocaine.
Pregnant and lactating mothers.
Individuals who have taken analgesics 12hrs before endodontic procedure.
Individuals under barbiturates and benzodiazepine medication.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method reduction in pain when injection site is precooled prior to the injection of the local anesthetic.Timepoint: the data will be measured based on the HP-VAS score before and after intervention.
- Secondary Outcome Measures
Name Time Method compare the effect of lignocaine gel in comparison to precooling of the anesthetic site prior to injection of the local anesthetic agent.Timepoint: the data will be measured based on the HP-VAS score before and after intervention.