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System safety verification and new technologies for clinical applications of tumor and cerebrovascular disease

System safety verification and new technologies for clinical applications of tumor and cerebrovascular disease

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054526
Enrollment
Unknown
Registered
2021-12-19
Start date
2021-12-11
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

Tumor and Vascular Disease

Interventions

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Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years, with the ability to act independently; 2. Agree to participate in this clinical trial and sign the informed consent; 3. One of the above-mentioned diseases is confirmed by clinical diagnosis.

Exclusion criteria

Exclusion criteria: 1. There are electronic implants, such as cardiac pacemakers, neurostimulators, insulin pumps, cochlear implants, etc.; 2. Those who have undergone aneurysm surgery and have intracranial aneurysm clips; 3. Those who have had heart surgery and have artificial heart valves; 4. There is a metal foreign body in the eye; 5. Metal implants and prostheses, or metal foreign bodies in other parts of the human body; 6. Women who are pregnant or have a pregnancy plan within three months, and are breastfeeding; 7. Critically ill patients who need to use a life support system; 8. Epilepsy patients and mentally ill patients; 9. Patients with claustrophobia; 10. History of previous allergic reaction to contrast agent, history of bronchial asthma, or other allergic diseases; 11. Acute or chronic severe renal injury (GFR < 30ml/min/1.73m2) or acute renal insufficiency caused by hepatorenal syndrome/perioperative period of liver transplantation; 12. Patients with known QT interval prolongation, patients with hypokalemia, receiving class IA (such as quinidine, procainamide) or class III (amiodarone, sotalol) antiarrhythmic drug patients; 13. Other situations in which the clinical trial investigators deem it inappropriate to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;

Countries

China

Contacts

Public ContactXu Haibo

Zhongnan Hospital of Wuhan University

zn002938@whu.edu.cn+86 15871692139

Outcome results

None listed

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