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Infusion norepinephrine versus infusion phenylephrine for prevention of hypotension after spinal anaesthesia in elective cesarean section.

Norepinephrine versus phenylephrine infusion for prevention of hypotension after spinal anaesthesia in elective cesarean section-A randomised double blinded study. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059859
Enrollment
60
Registered
2023-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O759- Complication of labor and delivery, unspecified Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Inj. Norepinephrine: After subarachnoid block with inj. bupivacaine 0.5%(H)2ml, inj. norepinephrine 8mcg/ml at the rate of 24ml/hr will be administered until the extraction of fetus Con

Sponsors

JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Parturients of ASA-2 with no comorbidities. -Height:150-170cm -Undergoing elective cesarean under spinal anaesthesia

Exclusion criteria

Exclusion criteria: -BMI >30kg/m2 -Patients with cardiac comorbidities: a. Rheumatic heart disease b. Coronary artery disease c. Hypertensive disorders of pregnancy. -Allergic reaction to local anesthetics or any history of allergy to local anaesthetics.

Design outcomes

Primary

MeasureTime frame
To compare the changes in maternal heart and blood pressure following infusions of norepinephrine versus phenylephrine.Timepoint: Starts as soon as subarachnoid block is given and terminated on the delivery of the baby

Secondary

MeasureTime frame
.To study the of incidence of hypotension and bradycardia. -To analyse the number of rescue doses of vasopressors used . -To record the APGAR score of neonates at 1 minute and 5 minutes. -To analyse the incidence of intra operative nausea and vomiting. Timepoint: Starts as soon as subarachnoid block is given and terminated on the delivery of the baby

Countries

India

Contacts

Public ContactDR CAPTAIN GURUDATT CL

JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH

dattguru55@gmail.com9845312311

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026