Pre-operative pain relief for fracture femur
Phase 4
- Conditions
- Health Condition 1: null- Patients with fracture femur between 18 to 70 years
- Registration Number
- CTRI/2018/01/011435
- Lead Sponsor
- TMMC LTMGH SION HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with either sex between 18 to 70 years with fraacture neck femur
Americaan Society of Aaesthesiologists Class I II and III
Exclusion Criteria
1.Patient refusal
2.Anticoagulation
3.Previous femoral bypass surgery
4.Inflammation or infection over injection site
5.Allergy to local anaesthetics
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of analgesia during positioning for central neuraxial blockade which will be assessed using <br/ ><br>Visual analogue score (VAS) pre block and post block ( before, during and after positioning) (Subjective assessment) <br/ ><br>Pain free range of passive flexion of the leg using goniometer (Functional assessment) <br/ ><br>Timepoint: It will be assessed till patients is given sitting position for spinal anaesthesia <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Time needed for central neuraxial blockade <br/ ><br>2.Time required for positioning <br/ ><br>3.Quality of patient positioning for central neuraxial blockade. <br/ ><br>4.Total dose of supplemental epidural drug required <br/ ><br>5.Side effects, if any <br/ ><br>Timepoint: 1,2 and 3 outcome will be assessed intraoperatively and 4 and 5 will be assessed intraoperatively as well as post-operatively