A comparative clinical trial to assess the effectiveness of two doses of bupivacaine in PENG block for relieving pain during hip fracture surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/03/040748
- Lead Sponsor
- Dr RP Govt Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
The study shall be conducted on 60 consecutive patients belonging to 40â??90 years of age range, American Society of Anaesthesiology Grade I/III and with a body mass index (BMI) of 18.5â??29.9 kg/m2.
Exclusion Criteria
Patient refusal for spinal anaesthesia, infection at the puncture site, coagulopathies, neuropathies, and any other contraindication to neuraxial block will be excluded from this study. Parturient patients and those with BMI of >30 kg/m2 will also be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the ease of sitting for the conduct of regional anaesthesia (graded as: 0-not satisfactory, 1-satisfactory, 2-good and 3-optimal) <br/ ><br>Timepoint: After 20 minutes (T 20) of application/institution of PENG block <br/ ><br>
- Secondary Outcome Measures
Name Time Method The pain assessment after the block utilizing VAS score.Timepoint: At 10 min and 20 min.