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Volume management guided by venae cava inferior collapse index preoperative can alleviate the spinal anesthesia inducted hypotension for elective Caesarean. A prospective randomized controlled study

Volume management guided by venae cava inferior collapse index preoperative can alleviate the spinal anesthesia inducted hypotension for elective Caesarean. A prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085758
Enrollment
Unknown
Registered
2024-06-18
Start date
2024-06-20
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

spinal anesthesia inducted hypotension

Interventions

US group:The maximum (IVCDmax) and minimum (IVCDmin) diameters of the IVC were measured respectively over the same respiratory cycle. The IVCCI was derived from the formula:IVCCI =(IVCDmax -IVCDmin)/I
C group:standard volume management

Sponsors

The Central People's Hospital of Yichang City, Hubei Province /The First Clinical Medical College, Three Gorges University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women aged 18 to 45 years old, with American Society of Anesthesiologists grade II or III, Pregnant age: 37-42 weeks;planned for elective caesarean section in The Central People's Hospital of Yichang City were included

Exclusion criteria

Exclusion criteria: The exclusion criteria were as follows: (1)Untreated underlying disease such as hypertension, diabetes, chronic pain, epilepsy, asthma, renal function impairment (BUN and or Cr> 2 times normal), liver function impairment (ALT and or AST> 1.5 times normal), ; (2)Combined with special obstetric conditions: placental abruption, placenta previa with bleeding, fetal abnormalities, twins or multiple pregnancy; (3)Pregnant women who need an emergency caesarean section due to special circumstances, such as fever with acute infection, trauma, premature rupture of membranes with fetal distress, etc.; (4) Pregnant women with allergies to any anesthetic component. (5) patients refused to participate in the study were excluded.(6)Patients with other conditions that the investigator considers are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
mean arterial blood pressure;the duration of the hypotension;inferior vena cava diameter(Maximum and minimum diameters of one respiratory cycle);postoperative recovery scores;

Secondary

MeasureTime frame
Blood gas analysis of umbilical cord blood;infusion quantity;Total dose of viable vascular drug (norepinephrine);

Countries

China

Contacts

Public ContactYuan Gong

The Central People's Hospital of Yichang City, Hubei Province,The School of Basic Medicine, Three Gorges University, Yichang City, Hubei Province

gy-yc@163.com+86 139 8674 6821

Outcome results

None listed

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