Health Condition 1: null- women for cesarean section
Conditions
Interventions
Intervention1: Women randomized to this group will receive hyperbaric bupivacaine with magnesium sulphate .: Women randomized to this group will receive 8 mg (1.6 ml) of 0.5% hyperbaric bupivacaine wi
Sponsors
Govt of Himachal Pradesh
Eligibility
Inclusion criteria
Inclusion criteria: • Singleton pregnancy • Woman for cesarean section as per obstetrical indication • Period of gestation between 36 to 41 weeks
Exclusion criteria
Exclusion criteria: • American society of Anesthesiologist grade >II • Renal or hepatic impairment • Thrombocytopenia • HELLP syndrome • Patient on magnesium therapy • Acute fetal distress • Contraindications to spinal anesthesia • Morbid Obesity (BMI > 38 kg/m 2) • Sensitivity to local anesthetic drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be the duration of spinal anesthesia in the study groups.Timepoint: six months | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢ Time taken for onset of sensory block â?¢ Time taken for onset of motor block â?¢ Time taken to achieve maximal sensory block â?¢ Duration of sensory block â?¢ Duration of motor block â?¢ Need and amount of rescue analgesia Timepoint: â?¢ Time taken for onset of sensory block â?¢ Time taken for onset of motor block â?¢ Time taken to achieve maximal sensory block â?¢ Duration of sensory block â?¢ Duration of motor block â?¢ Need and amount of rescue analgesia | — |
Countries
India
Contacts
Public ContactChanderdeep Sharma
Dr RPGMC Kangra
Outcome results
None listed