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Norepinephrine and Phenylephrine for Spinal Anesthesia-induced Hypotension.

NCT06508359 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 700

Last updated 2026-04-28

No results posted yet for this study

Summary

This study aims to explore the effects of different application modes (prophylactic and rescue strategy) of norepinephrine and norepinephrine on neonate umbilical artery pH undergoing cesarean section.

Conditions

  • Outcome

Interventions

DRUG

Norepinephrine

Prophylactic or rescue norepinephrine for spinal anesthesia-induced hypotension

DRUG

Phenylephrine

Prophylactic or rescue phenylephrine for spinal anesthesia-induced hypotension

Sponsors & Collaborators

  • General Hospital of Ningxia Medical University

    lead OTHER

Principal Investigators

  • Yi Chen, M.D. · General Hospital of Ningxia Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-01
Primary Completion
2026-04-21
Completion
2026-04-21

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06508359 on ClinicalTrials.gov