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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorThe First Affiliated Hospital with Nanjing Medical University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

pAVM with flow-related aneurysms were identified by DSA, and subarachnoid hemorrhage was confirmed by CT

No history of stroke, Marfan syndrome, polycystic kidney disease

Disqualifiers

pAVM without flow-related aneurysms

Absence of clinical data

Trial population

Patients with posterior circulation malformations combined with ruptured or unruptured flow-related aneurysms will be included. Morphological data such as aneurysm size, location, parent artery, feeding arteries, draining vein count, malformation size, malformation location, and the ratio of malformation/aneurysm volume will be analyzed. These factors will be examined alongside medical histories of hypertension, diabetes, and coronary artery disease to investigate the risk factors for ruptured flow-related aneurysms.

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 2 trial groups
Group A: pAVM with ruptured flow-related aneurysm
Group B: pAVM without ruptured flow-related aneurysm

Trial outcomes

Primary outcomes

1

characteristics of flow-related aneurysm

size ratio(aneurysm depth (mm)/parent artery diameter (mm))

Time frame
From enrollment to the end of treatment at 8 weeks

Secondary outcomes

Other outcomes

1

demographic information of pAVM-rFA

gender

Time frame
From enrollment to the end of treatment at 8 weeks
2

demographic information

age when be hospitalized

Time frame
From enrollment to the end of treatment at 8 weeks
3

characteristics of flow-related aneurysm

aspect ratio (aneurysm depth (mm)/aneurysm neck (mm))

Time frame
From enrollment to the end of treatment at 8 weeks
4

characteristic of avm

avm location

Time frame
From enrollment to the end of treatment at 8 weeks

Sponsors and contacts

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