Health Condition 1: O- Medical and Surgical Health Condition 2: 1- Obstetrics Health Condition 3: 1- Obstetrics
Conditions
Interventions
Intervention1: Height based group: Patients to recieve height adjusted dose(0.06mg/cm) of 0.5% heavy bupivacaine intrathecally via spinal needle at the time of induction before caesarean section
Contr
Sponsors
Rajendra Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patient consent 2.Age group - 21years to 40years scheduled for elective caesarean section 3.singleton pregnancy 4.Weight -40 to 80 kg 5.Height- 140cm-170cm 5.ASA II
Exclusion criteria
Exclusion criteria: 1.patient refusal 2.patient with contraindication to spinal anaesthesia 3.patient with cardiovascular disease,pre eclampsia,eclampsia and systolic BP 4.Women with fetal abnormalities 5.women with placental abnormalities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Incidence of maternal hypotension 2.Time to reach T8 sensory level 3.Maximum sensory level achieved and time to reach the same 4.Time taken for 2 segment sensory regression 5.Time to achieve modified bromage score 3 Timepoint: 24 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Total dose of mephentermine consumption 2.APGAR score at 1 and 5 min 3.To study side effects such as nausea, vomiting ,headacheTimepoint: 24 hrs | — |
Countries
India
Contacts
Public ContactDr Ekramul Haque
RIMS,Ranchi
Outcome results
None listed