CTRI/2019/08/020849RecruitingPhase 3
Comparison of Norepinephrine Infusion and Bolus Regimens During Cesarean Delivery Under Spinal Anesthesia: A Randomized Clinical Trial - NEIB
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Elective CS under spinal anaesthesia
- •2.Normal singleton pregnancy beyond 36
- •weeks gestation
- •3.ASA physical status 1 or 2
- •4. Weight 50-100 kg
- •5.Height 150-180 cm
Exclusion Criteria
- •1.Allergy or hypersensitivity to norepinephrine
- •2.Any hypertensive disorders of pregnancy
- •3.Cardiovascular or cerebrovascular disease
- •4.Fetal abnormalities
Investigators
Similar Trials
Not yet recruiting
Not Applicable
A comparison of dosage of norepinephrine drug and phenylephrine drug in the treatment of low blood pressure during spinal anaesthesia for caesarean sectioCTRI/2022/01/039587DR RESHMA BALAKRISHNA
Completed
Phase 2
To compare the effects of two drug inj. phenylephrine and inj.noradrenaline to control hypotension after spinal anaesthesia in lscs patient.CTRI/2021/02/031334Sumitha60
Not yet recruiting
Phase 4
Which of the two doses of norepinephrine (a drug to increase blood pressure) will better prevent hypotension (decrease in blood pressure) in pregnant women following spinal anesthesia undergoing emergency c-section?CTRI/2024/06/069181All India Institute of Medical Sciences, Bihar
Not yet recruiting
Phase 4
To compare the effect of phenylephrine and noradrenaline given for treatment for fall in blood pressure following spinal anaesthesia during caesarean delivery in pregnant patients with high blood pressureCTRI/2022/08/044968Dr Trina Sen
Recruiting
Phase 2
The effect of bolus injection of phenylephrine and norepinephrine in preventing hypotension after spinal anesthesia in patients undergoing elective cesarean elective.IRCT20080921001264N13Gorgan University of Medical Sciences90