Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients scheduled for elective lower limb orthopaedic surgeries under subarachnoid block. 2. ASA class I and II 3. Age 18-60 years 4. Height 150-170 cm 5. BMI 6. Both genders
Exclusion criteria
Exclusion criteria: 1. Patient refusal to participate in study 2. Infection at the site of injection of spinal anaesthesia 3. Patient having history of drug allergy to local anaesthetic and buprenorphine . 4. Patient having any deformities of the spine 5. Patient receiving steroids, analgesics and sedatives. 6. Patient with history of chronic pain. 7. Patient having history of endocrine, cardiovascular, renal or CNS disease. 8. Patient having history of bleeding disorder. 9. Patient having history of psychiatric disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the duration of postoperative analgesia of Intrathecal Ropivacaine Heavy with or without Buprenorphine in lower limb orthopaedic surgeriesTimepoint: upto 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the effect of Intrathecal Ropivacaine Heavy with or without Buprenorphine on postoperative analgesia in lower limb orthopaedic surgeries with regard to: 1. Onset of sensory block and motor block 2. Duration of sensory block and motor block. 3. Heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP) and Mean arterial pressure (MAP) 4. Side effects (a) Nausea and vomiting (b) Urinary retention (c) Sedation (d) Respiratory depressionTimepoint: upto 24 hours | — |
Countries
India
Contacts
school of medical sciences and research