to study the effectiveness of mannitol with routine local anesthesia in nerve blocks
Phase 4
- Registration Number
- CTRI/2022/10/046921
- Lead Sponsor
- radhika singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Individuals between the ages of 16 and 35 years who have no allergy to mannitol and lidocaine will be included in the study.
2.Individuals who require bilateral local anesthetic nerve blocks within same arch.
Exclusion Criteria
1.Subjects allergic to mannitol or lidocaine or with any underlying systemic disease or history of significant medication that would alter pain perception.
2.Pregnant and lactating mothers will be excluded from the study.
3.Patients with restricted mouth opening/ difficulty in mouth opening will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method