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Subclavian vein ultrasound-guided fluid replacement during cesarean section to prevent hypotension after spinal anesthesia: a randomized controlled study

Subclavian vein ultrasound-guided fluid replacement during cesarean section to prevent hypotension after spinal anesthesia: a randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100055050
Enrollment
Unknown
Registered
2021-12-31
Start date
2022-01-10
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

hypotension after spinal anesthesia

Interventions

Group 1:Subclavian Vein Collapse Index to Guide Fluid Rehydration
Group 2:Routine Rehydration

Sponsors

Shanghai First Maternity and Infant Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Full-term (>37 weeks), singleton, ASA I or II, elective cesarean delivery.

Exclusion criteria

Exclusion criteria: 1. There are contraindications to spinal anesthesia (such as low platelets caused by blood diseases, coagulation dysfunction, long-term use of anticoagulants, spinal deformity, history of lumbar spine surgery, infection at the puncture site, emotional instability and inability to cooperate, etc.); 2. Past or new heart disease, pre-eclampsia, neurological dysfunction, diabetes, cardiovascular and cerebrovascular or kidney disease, systolic blood pressure <90mmHg.

Design outcomes

Primary

MeasureTime frame
hypotension after spinal anesthesia;

Secondary

MeasureTime frame
fluid volume;nausea and vomiting;Neonatal Apgar Score;

Countries

China

Contacts

Public ContactLu Yan

Shanghai First Maternity and Infant Health Hospital

aneyan_lu@163.com+86 13162901723

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026