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A randomized controlled trial for comparing the effect and outcomes with different embolic agent: Absolute Ethanol and Onyx in the treatment of AVM

A randomized controlled trial for comparing the effect and outcomes with different embolic agent: Absolute Ethanol and Onyx in the treatment of AVM

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036576
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

arteriovenous malformations

Interventions

Group 1:absolute ethanol
Group 2:Oynx

Sponsors

Shanghai Ninth People Hospital, School of Medicine, Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) There was no history of AVMs treatment, including intervention and surgery. (2) According to the diagnostic criteria of AVMs, arteriovenous shunt and abnormal vascular mass were found. (3) Patients with good compliance and no contraindications. (4) There were imaging findings. (5) The patients and their families agreed and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnant and lactating women, history of drug allergy, liver and kidney dysfunction, heart and lung dysfunction. (2) After treatment, the patients who did not meet the design requirements or may affect the test results, such as misdiagnosis of arteriovenous malformation, were carefully differentiated. (3) The subjects dropped out. (4) Patients who quit the experiment before the end of treatment, such as death, automatic discharge, etc. (5) In the course of treatment allergic acute attack cases. (6) If the course of treatment is not over, the patient withdraws from the trial or dies due to other reasons. (7) Those who could not be followed up and naturally separated during observation.

Design outcomes

Primary

MeasureTime frame
the rate of nidus;

Secondary

MeasureTime frame
recurrence rate;Incidence of complications;

Countries

China

Contacts

Public ContactXindong Fan

Shanghai Ninth People Hospital, School of Medicine, Shanghai Jiaotong University

wdmdeming@hotmail.com+86 21-63231699

Outcome results

None listed

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