Comapring two techniques for Anesthesia of arm and forearm and their effect on respiratio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/10/037166
- Lead Sponsor
- PGIMER
- 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 scheduled to undergo upper limb surgeries under brachial plexus block
Exclusion Criteria
1. Patients with history og coagulopathy
2. Patient who refuse to give consent
3. Allergic to study drugs
4. Morbidly obese
5. Infection at intervention site
6. Neurological disease
7. Patient with psychiatric disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ipsilateral hemidiaphragmatic (during normal breathing,deep breathing and sniff manoeuvre) excursion at 30 minutes after brachial plexus blockTimepoint: T0- Pre block <br/ ><br>T30- 30minutes post block
- Secondary Outcome Measures
Name Time Method 1. Block onset time <br/ ><br>2. Block performance time <br/ ><br>3. Time to first rescue analgesia <br/ ><br>4. 24 hour rescue analgesic consumptionTimepoint: Pre block and measurements recorded every 5 minutes till 30 minutes post block <br/ ><br>Rescue analgesia seen upto 24 hours post surgery <br/ ><br>