Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Intervention1: Hyperbaric Ropivacaine 0.75%: Hyperbaric Ropivacaine 0.75% Alone in 1st group who are going undergoing Caesarean Section in 1 year
Control Intervention1: Hyperbaric Ropivacaine 0.75% wi
Sponsors
Dr Prachi
Eligibility
Inclusion criteria
Inclusion criteria: 1.Pregnant women scheduled for cesarean section 2.American Society of Anesthesiologists (ASA) physical status I or II
Exclusion criteria
Exclusion criteria: 1.Patients with contraindications to spinal anesthesia or opioids 2.ASA physical status III or higher 3.Patients with a history of opioid dependence or chronic pain syndromes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hyperbaric ropivacaine 0.75% with Fentanyl in Spinal Anesthesia Caesarean Section found to have longer duration of sensory and motor blockage then hyperbaric ropivacaine 0.75% aloneTimepoint: Primary outcome assessed in 5 minutes | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of subarachnoid block, hemodynamic stability,perioperative analgesia in patients undergoing Caesarean Section are better in patients receiving ropivacine 0.75% with fentanyl as compared to patients receiving ropivacine 0.75% aloneTimepoint: secondary outcome assessed in 1 hour | — |
Countries
India
Contacts
Public ContactDr Garima Chaurasia
Varun Arjun Medical College and Rohilkhand Hospital
Outcome results
None listed