A Clinical trial to study the effect of adding neostigmine to local anaesthetic ropivacaine for painless upper limb surgeries
Phase 2
- Conditions
- Health Condition 1: S699- Unspecified injury of wrist, handand finger(s)
- Registration Number
- CTRI/2024/05/067489
- Lead Sponsor
- M S Ramaiah Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anesthesiologists Physical status 1,2 and 3 undergoing elective upper limb surgeries.
Exclusion Criteria
Refusal to consent for the proposed study
Infection at injection site
History of any bleeding tendency, was taking oral anticoagulants(INR more than 1.5)
Brachial plexus-related neurological deficits
Allery to study drug
Chronic or Acute inflammatory conditions
Long term opioids/analgesics usage
Severe pulmonary/cardiac/hepatic disease
Epilepsy
Bronchial asthma
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess onset and length of sensory and motor blockadeTimepoint: 2,4,6,8,10,12,14,16 minutes and upto 24 hours for length
- Secondary Outcome Measures
Name Time Method To assess the intraoperative analgesic usage and postoperative analgesic need.Timepoint: 24 hours;To determine first analgesic request time and 24 hour total analgesic dosageTimepoint: 4,8,12,16,20,24 hours;To monitor occurrence of any side effectsTimepoint: 24 hours