Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Term parturients underwent elective LSCS under subarachnoid block 2. ASA grade I and II 3.Parturients giving written informed consent
Exclusion criteria
Exclusion criteria: parturients with BMI more than 30 Parturients with baseline systolic blood pressure less than 90mmHg. Parturients with pre-existing hypertension or pregnancy induced hypertension. Parturients with pre-existing major cardiovascular disease, respiratory disease Parturients with hepatic and renal dysfunction. Parturients with peripheral vascular disease. Parturients requiring conversion to general anaesthesia due to insufficient sensory block or failed spinal anaesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study is to compare the total fluid volume required in ultrasound guided subclavian vein fluid loading vs empirical fluid loading in parturients. Timepoint: Before induction of spinal anaesthesia and during intra-operative period. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To estimate pre-anaesthesia fluid requirement for prevention of post spinal hypotension in both the groups. 2. To compare the incidence of post-spinal hypotension in both the groups. 3.To estimate Intra operative mephentermine dosage requirement in both the groups. 4. To evaluate Intra operative changes in hemodynamic parameters (SBP,DBP,MAP, HR, SPO2) in both the groups. 5. To evaluate maternal adverse effects nausea, vomiting, bradycardia in both the groups. 6. To evaluate neonatal status (APGAR score) in both the groups.Timepoint: Before induction of spinal anaesthesia and during intra-operative period. | — |
Countries
India
Contacts
Pt. JNM Medical College Raipur CG