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Wearable continuous cardiac ultrasound guidance for optimizing fluid resuscitation in patients with septic shock

Wearable continuous cardiac ultrasound guidance for optimizing fluid resuscitation in patients with septic shock

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400095065
Enrollment
Unknown
Registered
2024-12-31
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Septic Shock

Interventions

CON group:ICU routine monitoring and liquid therapy
WCEM group:Wearable continuous cardiac ultrasound monitoring and personalized fluid resuscitation optimized treatment

Sponsors

Ziyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: septic shock, aged = 18 years.

Exclusion criteria

Exclusion criteria: Ultrasound cannot clearly display the inferior vena cava. Tricuspid regurgitation with or without right heart failure, right heart dysfunction. I have participated in other clinical trials in the past three months. Active blood loss, inferior vena cava reflux disorders, and contraindications to fluid replacement. Heart restriction, compression, thrombosis, venous filter implantation, ECMO channel establishment.

Design outcomes

Primary

MeasureTime frame
left ventricular function ;—

Secondary

MeasureTime frame
General Information;—

Countries

China

Contacts

Public ContactXiong Wei

Ziyang People's Hospital

xiongwei_1119@126.com+86 135 1835 3558

Outcome results

None listed

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