Pain relieving block for patients of hernia surgery.
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: null- Patients who are undergoing unilateral open inguinal hernia surgeries of ASA grade 1 and 2.
- Registration Number
- CTRI/2018/02/012011
- Lead Sponsor
- Government Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
1. ASA physical status I-II of both sexes.
2. Age between 18 to 80 years.
3. BMI >= 20 to <= 35 kg. m-2.
4. Scheduled for unilateral uncomplicated inguinal hernia surgery.
1. Patient refusal for the study
2. Patients having history of substance abuse
3. Contraindication to spinal anaesthesia
4. Contraindication or allergy to local anaesthetics and tramadol
5. Pregnant and lactating women
6. Inability to understand functioning of PCA pump and VAS (visual analogue scale).
7. Infection at local surgical site.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tramadol-sparing effect of quadratus lumborum (QL) block in post operative <br/ ><br>open inguinal hernia surgery patients.Timepoint: Post block,5,10,15minutes,1,4,8,12,18 and 24hr.
- Secondary Outcome Measures
Name Time Method 1.postoperative pain relief using visual <br/ ><br> analogue scale both at rest and movement. <br/ ><br>2.haemodynamics(PR,BP and RR) <br/ ><br>3.patient satisfaction score. <br/ ><br>4.nausea and vomiting. <br/ ><br>5.any other adverse effects.Timepoint: 1.Post block,5, 10,15 minutes ,1, 4, <br/ ><br> 8,12, 18,24 hrs and 3months.. <br/ ><br>2 Post block,5, 10,15 minutes ,1, 4, <br/ ><br> 8,12, 18 and 24 hrs postoperatively. <br/ ><br>3 At 24 hrs postoperatively and at 3 <br/ ><br> months. <br/ ><br>4.Post block,5, 10,15 minutes ,1, 4, <br/ ><br> 8,12, 18 and 24 hrs postoperatively. <br/ ><br>5.Post block,5, 10,15 minutes ,1, 4, <br/ ><br> 8,12, 18,24 hrs and 3months.