Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients of ASA 1 to 3 Physical status Patients undergoing caesarean section
Exclusion criteria
Exclusion criteria: Patients refusal for spinal anaesthesia Infection at site of spinal needle insertion Patients having allergy to local anaesthetic drugs Coagulopathy or Bleeding disorders Increased Intracranial pressure Any other relative contraindication of spinal anaesthesia Any renal disorder like CRF
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the hemodynamic stability of isobaric levobupivacaine plus fentanyl with isobaric ropivacaine plus fentanyl in caesarean sectionsTimepoint: 75 Minutes | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess onset and duration of sensory block, motor block and duration of analgesia by isobaric solutions of levobupivacaine and isobaric solutions of ropivacaine with addition of fentanyl To assess requirement of post operative analgesic drugs in patients undergoing caesarean section after administration of isobaric levobupivacaine and isobaric ropivacaine in caesarean sections Timepoint: Post Operative upto 1 hour | — |
Countries
India
Contacts
Pramukh Swami Medical College Karamsad Anand Gujarat