Skip to content

Follow-up of intracranial aneurysms treated with the Surpass flow diverter: comparison of subtraction CTA and DSA. Part II: a retrospective selected case series.

Follow-up of intracranial aneurysms treated with the Surpass flow diverter: comparison of subtraction CTA and DSA. Part II: a retrospective selected case series. - Follow-up Surpass: sCTA vs DSA. Part II.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42403
Enrollment
10
Registered
2015-10-15
Start date
2016-02-29
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

vascular ectasia vessel wall protrusion

Interventions

None listed

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: adults (age: 18 to 80) with an unruptured intracranial aneurysm treated with Surpass.

Exclusion criteria

Exclusion criteria: subarachnoid hemorrhage, earlier coiled aneurysm, allergy (hypersensitivity to iobitridol, history of major immediate or delayed skin reaction to Iobitridol injection) or contraindication to contrast agent (manifest thyrotoxicosis, recent treatment with intravenous interleukin 2), use of nephrotoxic medicines (aminoglycosides, organoplatinum compounds, high doses of methotrexate, pentamidine, foscarnet, aciclovir, ganciclovir, valaciclovir, adefovir, cidofovir, tenofovir, vancomycin, amphotericin B, immunosuppressants such as ciclosporine or tacrolimus, ifosfamide), contraindication to CT scan, renal insufficiency, pregnancy, and age

Design outcomes

Primary

MeasureTime frame
The main parameter is the difference in the degree of aneurysm occlusion. This will be measured by: - Calculation of the aneurysm volume with residual contrast filling. - The Raymond classification.

Secondary

MeasureTime frame
Secondary parameters: The patency of the parent vessel will be measured on a 4-point scale. Complications will be registered.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)