A study comparing different techniques of anaesthetizing upper arm during surgery
Phase 3
- Conditions
- Health Condition 1: null- ASA PS I and II patients posted for forearm surgeries with a surgical duration more than one hour
- Registration Number
- CTRI/2018/05/014074
- Lead Sponsor
- Maulana Azad Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I and II patients between 20-50 years of age of either sex with BMI <= 30 kg/meter square who posted for elective forearm orthopedic surgery in supine position of more than one hour duration
Exclusion Criteria
Patients with psychological disorders, coagulopathies,known allergy to local anaesthetics, infection at the puncture site, neuropathy, nerve injury and opioid dependence
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success rate of the brachial pleaxus blockTimepoint: Any two of the dermatome supplied by radial, ulnar, median and musculocutaneous nerve, not having analgesia even after 30 minutes of drug injection
- Secondary Outcome Measures
Name Time Method Duration of blockTimepoint: From onset of analgesia to return of normal sensation and motor function;Onset of blockTimepoint: From injection of local anaesthetic to decreased sensation to pin prick in at least two dermatome supplied by radial, ulnar, median and musculocutaneous nerve