a comparison between continuous epidural infusion and multimodal analgesia for post operative pain relief in patients undergoing abdominal hysterectomy
Not Applicable
- Conditions
- Health Condition 1: N80-N98- Noninflammatory disorders of female genital tract
- Registration Number
- CTRI/2019/03/017902
- Lead Sponsor
- J Arunashreya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing abdominal hysterectomy under spinal anaesthesia
Patient undergoing abdominal hysterectomy less than 60 yrs of age
American Society of Anesthesiologists (ASA) Physical Status (PS) I and II
Willingness to participate in the study
Exclusion Criteria
Patient refusal for epidural catheter placement or tap block
Body mass index (BMI) <18 and >30
Coagulation disorders and thrombocytopenia with platelet count <150,00
Infection at the site of injection and insertion of needle
 Patient on regular NSAIDS or opioids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare pain scores at the end of 24 hrs between two groupsTimepoint: end of 24 hours
- Secondary Outcome Measures
Name Time Method To compare pain scores, sedation and hemodynamic status between 2 groups at 4, 8,12,16,20 hrs after surgeryTimepoint: To compare pain scores, sedation and hemodynamic status between 2 groups at 4, 8,12,16,20 hrs after surgery