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Comparison of the Effect of Norepinephrine and Ephedrine Infusion on Stabilizing Blood Pressure and Hemodynamics during Cesarean Section under Spinal Anesthesia

Comparison of the Effect of Norepinephrine and Ephedrine Infusion on Stabilizing Blood Pressure and Hemodynamics of Mother Candidates for Cesarean Section under Spinal Anesthesia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120624010102N4
Enrollment
100
Registered
2024-09-17
Start date
2024-08-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Pregnancy, candidate for caesarean section, under spinal anesthesia. Other complications of spinal and epidural anesthesia during pregnancy

Interventions

Intervention 1: Intervention group: receiving ephedrine as an infusion of 1 mg/kg/minute. Intervention 2: Intervention group: receiving norepinephrine as an infusion of 0.05 µg/kg/min.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All Pregnant Mothers Cesarian Candidate Under Spinal Anesthesia ASA Class of One and Two

Exclusion criteria

Exclusion criteria: History of any underlying disease, including heart disease, kidney disease, diabetes, etc.

Design outcomes

Primary

MeasureTime frame
Mother Heart Rate. Timepoint: At the beginning and during surgery, every three minutes until the placenta is removed. Method of measurement: Monitoring Device.;Fetus Heart Rate. Timepoint: At the beginning and during surgery, every three minutes until the placenta is removed. Method of measurement: Monitoring Device.;Maternal Mean Arterial Pressure. Timepoint: At the beginning and during surgery, every three minutes until the placenta is removed. Method of measurement: Monitoring Device.;Maternal Blood Oxygen Saturation. Timepoint: At the beginning and during surgery, every three minutes until the placenta is removed. Method of measurement: Monitoring Device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSanaz Rajabloo

Tehran University of Medical Sciences

sanaz.rj@gmail.com+98 21 6634 8500

Outcome results

None listed

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