Health Condition 1: K257- Chronic gastric ulcer without hemorrhage or perforation
Conditions
Interventions
Intervention1: Ultrasound guided rectus sheath block will be given using Ropivacaine or Bupivacaine.: It is a Two-arm (parallel-group) randomized controlled trial. Two intervention groups are Group R:
Sponsors
Dr Subhajit paul
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA physical status 1 and 2. 2. Aged between18 65 years of old of either sex. 3. Patients undergoing abdominal surgeries with midline incision
Exclusion criteria
Exclusion criteria: 1. Refusal to consent 2. Known coagulopathy 3. Skin Infection / wound at the site of needle insertion. 4. History of allergy to study drugs. 5. Inability to understand and use Visual Analog Scale (VAS). 6. Patients having chronic kidney disease. 7. If patients require ventilator support postoperatively. 8. Surgery with anticipated duration of less than 2 hours will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the time to first rescue analgesia in the postoperative period between the two groups receiving ultrasound-guided rectus sheath block using either ropivacaine or bupivacaineTimepoint: Duration of analgesia will be measured in the first twenty four hours of post operative period | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the cumulative dose of rescue analgesics in the first 24 hours of postoperative periodTimepoint: cumulative dose of rescue analgesics will be measured in the first 24 hours of postoperative period.;To compare adverse events, if anyTimepoint: Adverse events will be noted in both the groups in the first twenty four hours of post operative period | — |
Countries
India
Contacts
Public ContactDr Subhajit Paul
Institute of Post Graduate Medical Education And Research
Outcome results
None listed