Trial to find out least volume of local anaesthetic required to conduct an upper arm surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- patients ASA I or ASA II with upper arm fracture
- Registration Number
- CTRI/2017/05/008603
- Lead Sponsor
- Dr SN medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 52
Inclusion Criteria
patient ASA I or II posted for upper arm surgery
Exclusion Criteria
patient refusal
bleeding diasthesis
hypersensitivity to local anaesthetic
infection at site of injection
pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Minimum effective volume of ropivacaine for surgical anaesthesiaTimepoint: Duration of surgery(less than 3 hours)
- Secondary Outcome Measures
Name Time Method Duration of anagesia <br/ ><br>adverse effectTimepoint: VAS score (within 24 hrs.) <br/ ><br>clinical assessment (within 24 hrs.)