Actively Recruiting

All Genders
NCT07050381

The Risk Factors Related to Rupture Flow-related Aneurysms in Posterior AVM

Led by The First Affiliated Hospital with Nanjing Medical University · Updated on 2025-07-03

200

Participants Needed

2

Research Sites

80 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

AVMs have been reported to rupture at a formidable annual rate of 2% to 3% at natural progression, often resulting in longterm neurological deficits and poor functional outcomes.The reported risk of hemorrhagic presentation in patients with AVMs is 41% to 65%. While many studies suggest a correlation between higher hemorrhage risk and the concurrent presence of AVM and aneurysms, few authors have focused specifically on flow-related aneurysms alone. In many instances, the source of rupture is also unclear. Meta-analysis from 2016 suggested that 49.2% of hemorrhages were secondary to aneurysm rupture, 45% from AVM rupture, and 5.7% were undetermined.In a study of 302 patients, of which 52.6% had a hemorrhagic presentation, demonstrated a significant increase in rate of hemorrhage in those with flow-related aneurysms. Thus, it is necessary to figure out risk factors related to ruptured flow-related aneurysms in pAVM.

CONDITIONS

Official Title

The Risk Factors Related to Rupture Flow-related Aneurysms in Posterior AVM

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • pAVM with flow-related aneurysms identified by DSA
  • Subarachnoid hemorrhage confirmed by CT
  • No history of stroke
  • No Marfan syndrome
  • No polycystic kidney disease
Not Eligible

You will not qualify if you...

  • pAVM without flow-related aneurysms
  • Absence of clinical data

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Jiangsu Province Hospital

Nanjing, Jiangsu, China, 225500

Active, Not Recruiting

2

the First Affiliated Hospital of Nanjing Medical University

Nanjing, Jiangsu, China

Actively Recruiting

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Research Team

Y

Yifei Wang

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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