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Comparison of carotid artery ultrasonography and subclavian vein ultrasonography for predicting supine hypotension syndrome of parturient after spinal anesthesia

The combined prediction value of carotid artery and subclavian vein ultrasonography for supine hypotension syndrome of parturient after spinal anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092902
Enrollment
Unknown
Registered
2024-11-26
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

supine hypotension syndrome

Interventions

According to whether supine hypotension syndrome occurs, it is divided into S group and W group:NA

Sponsors

Wuhu maternal and child Health care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-40 years old; 2. Grade I to II by the American Society of Anesthesiologists (ASA); 3. 37 ~ 42 weeks of pregnancy; 4. Single pregnancy.

Exclusion criteria

Exclusion criteria: 1. American Society of Anesthesiologists (ASA) grade III to IV; 2. Morbid obesity, BMI>40 kg/m^2; 3. non-sinus rhythm; 4. Placenta previa, placental abruption, multiple pregnancy; 5. Preeclampsia or gestational hypertension, basal systolic blood pressure >140 mmHg or < 90 mmHg; 6. History of cardiovascular and cerebrovascular diseases; 7. Abnormal platelet, coagulation, liver and kidney function; 8. Emergency surgery; 9. There are neurological and mental diseases that do not cooperate and cannot communicate.

Design outcomes

Primary

MeasureTime frame
carotid artery corrected flow time;respirophasic variation in carotid artery blood flow peak velocity;subclavian vein collapsibility index;maximum diameter of subclavian vein;minimum diameter of subclavian vein;

Countries

China

Contacts

Public ContactRui Yan

Wuhu maternal and child Health care Hospital

1500812051@qq.com+86 188 9534 9102

Outcome results

None listed

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