Trial to find out minimum effective volume of local anaesthetic in ultrasound guided nerve block for forearm surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA Grade I-II
- Registration Number
- CTRI/2016/10/007370
- Lead Sponsor
- Dr Sampurnanand Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 29
Inclusion Criteria
ASA Grade I-II patients without any associated significant pathology (excluding criteria), posted for forearm surgery under above mentioned age group, were included in our study
Exclusion Criteria
a.Patientâ??s refusal.
b.Patients with history of bleeding disorders or patients on anticoagulants.
c.Patients with infection at the site of injection.
d.Patients with allergy to LA.
e.ASA grade 3 & 4 patients.
f.Anatomical abnormality at the regional site.
g.Neurodeficit involving brachial plexus.
h.Pregnant women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)minimum effective volume of ropivacaine <br/ ><br>2)duration of analgesia 3) adverse effects.Timepoint: assessment of block quality by calculatioin of composite score of bromage scale and duration of analgesia was recorded by patient response.
- Secondary Outcome Measures
Name Time Method /ATimepoint: N/A