A comparative study of 0.5% ropivacaine with combination of 0.5% bupivacaine and 2% lidocaine on intraocular pressure before and after peribulbar block in cataract surgery
Phase 4
- Conditions
- Health Condition 1: H251- Age-related nuclear cataractHealth Condition 2: H251- Age-related nuclear cataract
- Registration Number
- CTRI/2024/03/064131
- Lead Sponsor
- BLDE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Uncomplicated cataract.
2)Normal intraocular pressure
Exclusion Criteria
1)Patients with cognitive impairment.
2)Patients allergic to hyaluronidase, lidocaine, ropivacaine and bupivacaine.
3)Any other surgeries combined with cataract.
4)Patients with hypertension and coronary artery disease in lignocaine group.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)The study will help us to study the adverse effects caused by raised intra ocular pressure post peribulbar block and reduce the side effects caused by prolonged motor blockade by using a low concentrated anesthetic. <br/ ><br> <br/ ><br>2)This study will help us to know an ideal drug for peribulbar block with minimal complications. <br/ ><br>Timepoint: 31 cases in 6months and total 62 cases in 1 year <br/ ><br>
- Secondary Outcome Measures
Name Time Method This study will help us to know an ideal drug for peribulbar block with minimal complications. <br/ ><br>Timepoint: 31 cases in 6months and total 62 cases in 1 year <br/ ><br>