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To assess hemodynamic changes between preeclamptic versus healthy parturients undergoing elective cesarean section under spinal anaesthesia

Not Applicable
Conditions
Health Condition 1: O149- Unspecified pre-eclampsia
Registration Number
CTRI/2024/02/062962
Lead Sponsor
Department of anaesthesia Sawai Man Singh Medical College and Attached Hospital Jaipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient providing consent

Patient belonging to ASA II and III

Patient with preeclampsia BP more than 140/90 mmHg after 20 weeks of gestation and proteinuria more than plus 2

Exclusion Criteria

Non cooperative patient

Patient should not be part of any other study

Patient with contraindication to neuraxial anaesthesia

patient with cardiac diisease , chronic hypertension and gestational hypertension

Patient with renal disease , coagulopathy platelet count less than 80000 and high spinal

Patient with active labor , eclampsia , abruption placenta , placenta previa and twin pregnancy

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Change in intraoperative hemodynamic variables in terms of mean SBP , mean DBP , mean MAP (mmHg ) and mean HR (min) <br/ ><br>2. Difference in mean total dose of ephedrine required (mg) <br/ ><br>3. Difference in mean total amount of intraoperative fluid required (ml)Timepoint: 1. 00 min <br/ ><br>2. 2min <br/ ><br>3. 4min <br/ ><br>4. 6min <br/ ><br>6. 8min <br/ ><br>7. 10min <br/ ><br>8. 12min <br/ ><br>9. 14min <br/ ><br>10. 20min <br/ ><br>11. 25min <br/ ><br>12. 30min <br/ ><br>13. 35min <br/ ><br>14. 40min <br/ ><br>15. 45min <br/ ><br>16. 50min <br/ ><br>17. 55min <br/ ><br>18. 60min <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
ilTimepoint: Nil
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