to compare two adjuvant drugs combination for nerve block for upper limb surgery and postoperative pain relieve
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057701
- Lead Sponsor
- Swarnika Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Age- 18years to 80years
2.Both gender
3.American Society of Anesthesiologists classification 1-3
4.Body mass index between 20 and 35
1.Adults who are unable to give their own consent
2.Pre-existing neuropathy (assessed by history and physical examination)
3.Coagulopathy (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. platelets = 100, International Normalized Ratio = 1.4 or prothrombin time = 50)
4.Renal failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. creatinine = 100)
5.Hepatic failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. transaminases = 100)
6.Allergy to local anesthetics (LAs)
7.Pregnancy
8.Prior surgery in the infraclavicular region
9.Chronic pain syndromes requiring opioid intake at home
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Motor block durationTimepoint: 24-48 hours after block
- Secondary Outcome Measures
Name Time Method Block performance timeTimepoint: 1 hour before surgery;Sensory & analgesic block durationTimepoint: 24-48 hours after nerve block