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Comparison of effects in puerpera andfetus with norepinephrine andphenylephrine during a cesarean delivery: a prospective, double-blind, randomized, controlled trial

Comparison of effects in puerpera andfetus with norepinephrine andphenylephrine during a cesarean delivery: a prospective, double-blind, randomized, controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007173
Enrollment
Unknown
Registered
2015-10-06
Start date
2015-10-08
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

General surgery

Interventions

A:norepinephrine

Sponsors

Beijing YouAn Hospital, Capital Medial University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: ASA physical status I parturientes at full-term gestation, 18-45 yr of age, at term gestation (longer than 37 weeks) with a singleton uncomplicated pregnancy

Exclusion criteria

Exclusion criteria: Exclusion criteria included age younger than 16 years, height less than 150 cm or more than 180 cm, weight less than 50 kg or more than 100 kg, bleeding disorders, had hypertension, any hypertensive disease of pregnancy, diabetes mellitus, any contraindication to regional anesthesia, or an allergy to any of the study medications.

Design outcomes

Primary

MeasureTime frame
Cord Blood PH;Hypotension;Bradycardi;

Countries

China

Contacts

Public ContactZhe-feng Quan
15811190059@126.com+86 15811190059

Outcome results

None listed

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