A study of methodology and application of Ultrasound-guided Percutaneous Minimally Invasive Autopsy

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000031279

Enrollment

Unknown

Registered

2020-03-26

Start date

2020-03-25

Completion date

Unknown

Last updated

2020-03-30

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

Conditions

Ultrasound-guided Percutaneous Minimally Invasive Autopsy

Interventions

case series:Ultrasound guided percutaneous minimally invasive autopsy

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. In-hospital deaths case who have an autopsy requirement; 2. Their immediate relatives sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Clear clinical condition and cause of death; 2. Target organs can not be displayed by ultrasound; 3. Patients whose death time exceeds 48 hours.

Design outcomes

Primary

Measure	Time frame
sampling success rate;Adverse event;	—

Secondary

Measure	Time frame
sampling time-consuming;	—

Countries

china

Contacts

Public ContactMingxing Xie

Union Hospital affiliated to Tongji Medical College, Huazhong University of Science and Technology

xiemx@hust.edu.cn+86 13607108938

Outcome results

None listed

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