CTRI/2022/12/047845Not yet recruiting未知
A study to compare the effect of prophylactic infusion of two different doses of phenylephrine on maternal hypotension and neonatal outcome in females undergoing cesarean section under spinal anaesthesia.
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
- Department of Anaesthesia
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Patients with physical status ASA grade I or II.
- •2.All patients giving written informed consent.
- •3.Patients with gestation age > 36 weeks posted for elective caesarean delivery under spinal anaesthesia.
- •4.Patients belonging to age group of 18 to 35 years.
Exclusion Criteria
- •1.Parturients with complications like risk of excessive bleeding (placenta previa, prolonged labor, abnormal presentation, multiple gestation)
- •2.Patients with pre-existing or pregnancy induced hypertension or maternal SBP < 100mm Hg.
- •3.Patients with cardiovascular disease, cerebrovascular disease, severe anemia or diabetes.
- •4.Patients with known fetal abnormalities.
- •5.Patients with contraindication to spinal anaesthesia.
- •6.Patients with known allergy to phenylephrine
- •7.Patients with inability or refusal to give informed consent
Investigators
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