Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: American Society of Anesthesiologists ASA physical status I-II Except Pregnant or Lactating women Informed consent will be obtained from the patients for participating in the study
Exclusion criteria
Exclusion criteria: Patients with known allergies to Local Anesthesia Patients with contraindications to epidural anesthesia For example infection at the injection site and coagulopathy Patients with chronic pain conditions or on longterm opioid therapy Patients with neurological or psychiatric conditions that may interfere with pain assessment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To Compare the post operative analgesic effect after administration of epidural bupivacaine 0.125% and ropivacaine 0.1%Timepoint: From starting of infusion till 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To Determine the requirement for rescue analgesia postoperatively when patient is on Epidural infusionTimepoint: From starting of infusion till 24 hours | — |
Countries
India
Contacts
Varun Arjun Medical College and Rohilkhand Hospital