Comparing Post-Operative Pain Relief Between Lumbar Erector Spinae Plane Block And Psoas Compartment Block In Patients Undergoing One Sided Total Hip Replacement Surgery.
Not Applicable
- Conditions
- Health Condition 1: M169- Osteoarthritis of hip, unspecified
- Registration Number
- CTRI/2024/03/063483
- Lead Sponsor
- Sanjana Annie Mathew
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who will require unilateral total hip replacement and are willing to give
consent to take part in the study will be included.
Exclusion Criteria
Patients who refuse to give their consent
Age less than 18 Years
ASA 4 or above
Local anesthetic allergy
Local sepsis or infection at puncture site
Patients with bleeding diathesis
Patients with peripheral neuropathy
Patients with dementia
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umerical Pain Rating ScaleTimepoint: Every 12 hourly till 96 Hours
- Secondary Outcome Measures
Name Time Method The secondary objective is to assess <br/ ><br>1.Time To First Rescue Analgesic(TTRFA) <br/ ><br>2.Number of rescue analgesia consumed <br/ ><br>3.Time to ambulate <br/ ><br>4.Length of hospital stay <br/ ><br>5.Incidence of complicationsTimepoint: Every 12 hourly