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Prospective multicenter study of ultrasonic treatment of carotid atherosclerosis plaque ablation

Prospective study on the effect of carotid atherosclerosis plaque ablation by ultrasound

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TCC-14005068
Enrollment
Unknown
Registered
2014-08-06
Start date
2014-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Atherosclerosis

Interventions

research group:Ultrasound ablation

Sponsors

Department of Ultrasound, Xijing Hospital, the Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. To be aged 35 to 65 years old; 2. To be with bilateral or unilateral carotid atherosclerotic disease; 3. without carotid surgery operation, the history of interventional therapy in patients with ischemic encephalopathy; 4. ultrasound carotid artery plaque without ulcers and internal bleeding, the maximum thickness of plaque is more than 2mm, carotid artery stenosis rate of less than 50% patients; 5. no the heart, liver, kidney function was not complete; 6. patients (or guardian, lineal relatives) signed the informed consent of patients; 7. Patient who is considered to be suite for the study by the investigator.

Exclusion criteria

Exclusion criteria: 1. carotid surgery operation, the history of interventional therapy in patients with ischemic encephalopathy; 2. occurred within one year after cerebral infarction, transient ischemic attack patients; 3. occurred within one year after myocardial infarction and treated patients; 4. ipsilateral carotid artery severe tortuosity, difficult to obtain accurate measurement results; 5. patients with serious heart, liver, kidney dysfunction; 6. blood pressure higher than 180/100mmHg; 7. patients with bleeding tendency; 8. in critical condition and other condition that cannot complete carotid examination; 9. can not complete the prescribed course of protocol; 10. did not sign the informed consent.

Design outcomes

Primary

MeasureTime frame
The maximum thickness of plaque;Percent area stenosi;

Secondary

MeasureTime frame
Gray median;Vmax;

Countries

China

Contacts

Public ContactZhou Xiaodong
xdzhou@fmmu.edu.cn+86 029-84775447

Outcome results

None listed

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