study on prolongation of spinal analgesia using Inj Bupivacaine 0.5% (H) and Inj Bupivacaine 0.5% (H) with Inj Clonidine 60 µ as a single shot Intrathecal injection.
Phase 4
- Conditions
- Health Condition 1: null- Patients undergoing lower abdomen and lower limb surgeries
- Registration Number
- CTRI/2012/04/002556
- Lead Sponsor
- Peoples Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ASA Grade I & II patients undergoing lower abdomen and lower limb surgeries.
Exclusion Criteria
All the patients who have contraindications to spinal anesthesia will be excluded. Patients undergoing emergency surgeries and pregnant patients will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method motor block regession in bromage score,sensory block regession by pin prick senstion to dermatomes,time to requirement to first analgesic in post operative period,any other side effects like nausea,headache,itching etcTimepoint: 4 to 8 hours after intra thecal injection
- Secondary Outcome Measures
Name Time Method sensory block regession by pin prick senstion to dermatomes,time to requirement to first analgesic in post operative period, any other side effects like nausea,headache,itching etcTimepoint: nil