ltrasound guided infraclavicular brachial plexus block with 2 different approaches
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/05/067845
- Lead Sponsor
- Government medical college and new civil hospital Surat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients who will undergo planned upper limb surgeries under usg guided Infraclavicular brachial plexus block with Costoclavicular and Retroclavicular approaches and giving written informed consent.
2. Patients belonging to ASA class 1, 2,3 .
3.Patients of either sex, in the age group of 18 to 65yrs.
Exclusion Criteria
1. Patients with known hypersensitivity to local anaesthetics.
2. Infection at the site of block . 3. Morbidly obese patient.
4.Patients with neurological, psychiatric or neurovascular disorders.
5.Patients with major cardio-pulmonary or hepato renal compromise.
6. Pregnant patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Block performance time. <br/ ><br>2) Block characteristics- onset and duration of sensory and motor block <br/ ><br>3)Quality of block.Timepoint: 1) Block performance time will be assessed from time of needle insertion to time of injecting drug <br/ ><br>2) Block characteristics- onset and duration of sensory and motor block for 24 hours <br/ ><br>3)Quality of block.
- Secondary Outcome Measures
Name Time Method 1)Duration of post operative analgesia and requirement of analgesics in 24 hours. <br/ ><br>2)Intraoperative Hemodynamic changes. <br/ ><br>3)Complications/Adverse events if anyTimepoint: Till 24 hours after giving block