To study postoperative analgesia using Bupivacaine and Dexmedetomidine in Ultrasound guided fascia iliaca block in proximal end femur surgeries
Phase 4
- Conditions
- Health Condition 1: V00-Y99- External causes of morbidity
- Registration Number
- CTRI/2024/04/065371
- Lead Sponsor
- Department of anaesthesia sawai man singh medical college jaipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient undergoing elective surgery for fracture proximal end of femur.
2.Adult patients aged 20-60 Years.
3.Patients belonging to American Society Of Anesthesiologists(ASA) grade I, II.
4. Patients consenting to participate.
Exclusion Criteria
1. Patients included in other study
2.Non cooperative patient.
3. Patients with multi-trauma or fractures,
4.Patients on chronic opioid use or addiction
5. Contraindication to neuraxial anesthesia (e.g., coagulopathy, infection, etc.)
? Infection at the site of block
? Previous femoral bypass surgery or inguinal hernia
? History of allergy to local anesthetics or dexmedetomidine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Mean duration of analgesia <br/ ><br>2 Mean of NRS score preoperatively <br/ ><br>3.Mean of NRS score postoperatively <br/ ><br>4.Mean dose of analgesic required <br/ ><br>5.Median of sedation scoreTimepoint: Postoperative 1hr Postoperative 2hr Postoperative 6hr Postoperative 8hr Postoperative 12hr Postoperative 16hr <br/ ><br>Postoperative 20hr Postoperative 24hr
- Secondary Outcome Measures
Name Time Method 1.Mean systolic B.P, mean diastolic B.P, Mean of mean B.P, Mean heart rate <br/ ><br>2.Proportion of cases having adverse effects if any in both the groupsTimepoint: 0min 5min 10min 15min 20min 25min 30min