use of different anesthetic solutions in providing pain relief during root canal treatment
- Registration Number
- CTRI/2019/10/021593
- Lead Sponsor
- Faculty of Dentistry self funded
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 150
the inclusion criteria will be carious exposed symptomatic mandibular molars; a positive and prolonged response to thermal tests and electric pulp test; a vital coronal pulp on access opening; American Society of Anesthesiologists class I or II medical history; and the ability to understand the use of pain scales.
Exclusion criteria will be known allergy or contraindications to any content of local anesthetic solution, patients who are pregnant or breast-feeding, a history of known or suspected drug abuse, and patients taking any drugs which could affect the pain perception. Patients having active pain in more than 1 teeth will be excluded from the study. Teeth with fused roots, radiographic evidence of an extra root, large restorations with overhanging margins, gingival inflammation, full crowns or deep periodontal pockets will also be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome was defined as ââ?¬Å?success or failureââ?¬? which was indicated as the ability to undertake pulp access and canal instrumentation with no or mild pain.Timepoint: The primary outcome will be evaluated at the baseline
- Secondary Outcome Measures
Name Time Method The secondary outcome was the evaluation of heart rate (number of heart beats per minute) after injections.Timepoint: Just after giving intraligamentary injections