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Comparative analysis of wearable ultrasound technology and Flotrac in hemodynamic monitoring during renal transplantation

Comparative analysis of wearable ultrasound technology and Flotrac in hemodynamic monitoring during renal transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123592
Enrollment
Unknown
Registered
2026-04-28
Start date
2025-01-08
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

chronic kidney disease stage 5

Interventions

Simple ultrasound group:None
Ultrasound + Flotrac group:None

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. regardless of gender ; aged 18-65 years old; 2. American Society of Anesthesiologists anesthesia classification : III-IV; 3. Preoperative regular dialysis treatment; 4.The family members of the patients voluntarily signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.Preoperative severe cardiovascular diseases : severe arrhythmia, cardiac function grade III / IV, severe heart failure in the past 3 months, cardiac ejection fraction EF < 50 %, coronary atherosclerotic heart disease and severe heart valve disease; 2.Severe nervous system, liver, lung and other organ failure; 3.long-term use of sedative or antidepressants;patients with communication disorders such as neurological and mental disorders; 4. Patients with a history of allergy to anesthetics; 5.Acute pulmonary infection occurred before operation.

Design outcomes

Primary

MeasureTime frame
Cardiac output;Creatinine reduction ratio;Lactate levels;

Secondary

MeasureTime frame
Days of ICU stay;Postoperative morbidity;

Countries

China

Contacts

Public ContactXueke Du

The Second Affiliated Hospital of Guangxi Medical University

duxueke@gxmu.edu.cn+86 137 0788 8675

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026