A clinical study to determine the effectiveness of 2% lignocaine with varying concentration of adrenaline used in dental extraction procedures.
Phase 2
- Conditions
- Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified
- Registration Number
- CTRI/2022/07/044039
- Lead Sponsor
- Self Dr Namrata Patil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Individuals falling in 40-60 age group.
individuals needing maxillary molar/premolar extractions.
Individuals with controlled hypertension.
Exclusion Criteria
Individuals with known H/O of thyroid disorder, renal disease , uncontrolled hypertension ,under antiplatelets & anticoagulant therapy , bronchial asthma and pregnant females
Patients with known allergy to any of the study drugs.
Mentally challenged patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain measured by Visual Analog ScaleTimepoint: 5 minutes
- Secondary Outcome Measures
Name Time Method Blood pressureTimepoint: Mm of Hg by automated sphygmomanometer before and after LA injection and immediately after completion of the extraction procedure.;Need for suturingTimepoint: yes/no;PulseTimepoint: Beats per minute before and after injection of local anesthetic and immediately after extraction procedure;Volume of anesthetic agentTimepoint: ml