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Clinical trial of image fusion of color ultrasound diagnosis system

Clinical trial of image fusion of color ultrasound diagnosis system

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055689
Enrollment
Unknown
Registered
2022-01-16
Start date
2022-01-17
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Urinary diseases, hepatobiliary diseases

Interventions

Gold Standard:MyLab 8 eXP, a color ultrasound diagnostic system produced by ESAOTE S.p.A.
Index test:Venus 1, a color ultrasound diagnostic system produced by Caben (Shenzhen) Medical Instruments Co., Ltd.

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Has signed the informed consent; 2. Over 18 years old, liver, gallbladder and kidney ultrasonography are not limited to men and women, prostate ultrasound is limited to men; 3. Clinically completed or planned to undergo liver CT, kidney CT or prostate magnetic resonance within 2 weeks.

Exclusion criteria

Exclusion criteria: 1. Patients with nephrectomy or prostatectomy; 2. Patients with severe kyphosis or scoliosis; 3. Severe heart, lung, and brain diseases, who cannot tolerate long-term examination; 4. Lactating and pregnant women; 5. Those who have a history of mental illness, drug abuse, alcoholism or neurological diseases (such as convulsions, epilepsy, Parkinson's disease, etc.) or who cannot understand the requirements of participating in the research and are difficult to cooperate; 6. The researcher believes that the subject is not suitable to participate in this research.

Design outcomes

Primary

MeasureTime frame
Excellent rate of fused image;

Secondary

MeasureTime frame
Overall consistency rate of fused image;

Countries

China

Contacts

Public ContactYongqiang Zhan

Shenzhen Second People's Hospital

yqzhan@sina.com+86 13714096676

Outcome results

None listed

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