To compare the pain-relieving effect of nerve block in neck given before or after surgery in patients scheduled for upper limb surgeries
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/04/032756
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 28
Inclusion Criteria
1.American Society of Anesthesiologists(ASA) physical status I-II
2. Age 18-65 years
3. BMI 18-30 kg m-2
4. Both sexes
5.Scheduled for upper limb surgery
Exclusion Criteria
1. Patient refusing to give informed consent
2. History of relevant drug allergy
3. History of psychiatric illness, substance abuse
4. Severe cardiovascular, respiratory, metabolic or neurological disease
5. Pregnancy and lactation
6. Coagulopathy and bleeding disorders
7. Infection at the planned injection site
8. Inability to understand a pain visual analogue scale (VAS)
9. Chronic sympathetic-mediated pain syndromes affecting the upper limb or trauma other than to the affected limb.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to first rescue analgesiaTimepoint: in postoperative period up to 24 hours
- Secondary Outcome Measures
Name Time Method