Skip to content

Study of the ratio of norepinephrine and phenylephrine for preventing post spinal hypotension during cesarean section under combined spinal-epidural anesthesia

Study of the ratio of norepinephrine and phenylephrine for preventing post spinal hypotension during cesarean section under combined spinal-epidural anesthesia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056237
Enrollment
Unknown
Registered
2022-02-02
Start date
2022-02-14
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

hypotension

Interventions

Norepinephrine group (A):Preventative infusion of norepinephrine
Phenylephrine group (B):Prophylactic infusion of norepinephrine

Sponsors

Jiaxing Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I - II; 2. Aged 20 to 40 years: 3. Term (>=37 weeks), singleton, cephalic pregnant women who planned elective cesarean section.

Exclusion criteria

Exclusion criteria: 1. Contraindications for spinal nerve block; 2. Complicated with cardiovascular and cerebrovascular diseases, pregnancy-related hypertension, fetal distress and spinal anesthesia, twin and multiple pregnancies, etc.

Design outcomes

Primary

MeasureTime frame
blood pressure;

Secondary

MeasureTime frame
Fetal weight;Total amount of vasoactive drugs used;Highest level of anesthesia;Times of single infusion of vasoactive drugs;

Countries

China

Contacts

Public ContactXiao Fei

Jiaxing Maternal and Child Health Care Hospital

13706597501@163.com+86 13706597501

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026