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Spinal Dural Arteriovenous Fistula International Data and Outcomes Registry

SPIDER - Spinal Dural Arteriovenous Fistula International Data and Outcomes Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07574645
Acronym
SPIDER
Enrollment
1000
Registered
2026-05-08
Start date
2026-01-05
Completion date
2026-05-01
Last updated
2026-05-08

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

Conditions

Spinal Dural Arteriovenous Fistula

Keywords

spinal dural arteriovenous fistula, spinal arteriovenous malformation, spinal AVF, sdAVF, international, multicenter, registry

Brief summary

Given the lack of large multicenter datasets in the context of Spinal arteriovenous fistula, the strength of the evidence surrounding this rare disease is limited. SPIDER hence aims to address that by compiling patient-level data from centers all around the world.

Detailed description

Type 1 or dural spinal arteriovenous fistulas (SDAVFs) are the most common spinal vascular malformation but remain frequently underdiagnosed due to their insidious onset and nonspecific clinical presentation. Delayed diagnosis is common and often results in progressive, and sometimes irreversible, myelopathy. Despite advances in imaging and treatment, there remains significant variability in diagnostic timelines, treatment strategies (endovascular, surgical, or combined), and reported outcomes across institutions. Existing literature is largely limited to single-center retrospective series or small cohorts, often underpowered to evaluate predictors of outcome, recurrence, and the impact of diagnostic delay. Furthermore, direct comparisons between treatment modalities and long-term functional outcomes using standardized clinical scales are limited. The SPIDER registry is designed to address these gaps by creating the largest international, multicenter dataset of patients with spinal dural AVFs. By pooling de-identified data from high-volume centers worldwide, this study aims to provide robust, generalizable evidence to inform clinical decision-making and optimize patient outcomes.

Interventions

None listed

Sponsors

Thomas Jefferson University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Type 1 spinal dural arteriovenous fistula, confirmed on imaging * Surgically or endovascularly treated * At least 1 available primary outcome

Design outcomes

Primary

MeasureTime frameDescription
Treatment successRecorded at the end of the embolization or surgery.Complete surgical/endovascular obliteration of the fistula
RecurrenceTime-to-event Outcome Measures. Estimated period of time over which the event is assessed: on average 1.5 years after surgery.Fistula recurrence
Status of symptoms at last clinical follow-upTime-to-event Outcome Measures. Estimated period of time over which the event is assessed: on average 1.5 years after surgery.Improved, unchanged, or worsened pain, sensory, and motor symptoms
Modified Aminoff-Logue ScaleTime-to-event Outcome Measures. Estimated period of time over which the event is assessed: on average 1.5 years after surgery.Gait and bowel/bladder score
Modified Rankin ScaleTime-to-event Outcome Measures. Estimated period of time over which the event is assessed: on average 1.5 years after surgery.Measure of functional independence
MortalityTime-to-event Outcome Measures. Estimated period of time over which the event is assessed: on average 1.5 years after surgery.

Countries

United States

Contacts

CONTACTPascal Jabbour, MD
pascal.jabbour@jefferson.edu215-955-7000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026