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Effect of continuous lower limb compression on the dose of phenylephrine in cesarean section under spinal anesthesia

Effect of continuous lower limb compression on the dose of phenylephrine in cesarean section under spinal anesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072492
Enrollment
Unknown
Registered
2023-06-15
Start date
2023-06-15
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

Treatment of Hypotension

Interventions

Group P:Phenylephrine continuous infusion (25ug.min-1)
Group A:Continuous lower limb compression combined with phenylephrine infusion (25ug.min-1)

Sponsors

Women and Children's Hospital Affiliated to Jiaxing University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Term (=37 weeks) pregnant women, singleton pregnancy, head presentation, and those requiring elective cesarean section.

Exclusion criteria

Exclusion criteria: Combined with cardiovascular and cerebrovascular diseases, pregnancy-related hypertension, fetal intrauterine distress and spinal anesthesia contraindications

Design outcomes

Primary

MeasureTime frame
The amount of phenylephrine used;—

Secondary

MeasureTime frame
Incidence of Hypotension;Nausea and vomiting;Incidence of bradycardia;Incidence of fetal distress;Neonatal PH value;Lactic acid of newborn;neonatal weight;apgar scare;—

Countries

China

Contacts

Public Contactyao han qing

Women and Children's Hospital Affiliated to Jiaxing University

yhq20113956@163.com+86 158 8830 6435

Outcome results

None listed

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