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CLEOPATRA

Cost Effectiveness of CT Perfusion for Patients suffering from Acute Ischemic Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27029
Enrollment
1200
Registered
2019-08-19
Start date
2019-07-23
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Acute ischemic stroke

Interventions

The intervention is the acquisition of CTP in all patients undergoing evaluation for EVT at all intervention centers in the Netherlands. Infarct core size, penumbra size, core-penumbra mismatch and in

Sponsors

Leading the Change (LtC); ZonMW
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • A clinical diagnosis of acute ischemic stroke. • CT or MRI scan ruling out intracranial hemorrhage. • Extracranial carotid and intracranial arterial occlusion demonstrated with CTP and CTA, MRA or DSA. • Intracranial proximal arterial occlusion of the anterior circulation (intracranial carotid artery (ICA, ICA-T) or middle (M1/M2) or anterior (A1/A2) cerebral artery), demonstrated by CTA, MRA or DSA. • Endovascular treatment was initiated; defined as groin puncture. • Age of 18 or above. • A score of at least 2 on the NIH Stroke Scale. • Written informed consent.

Exclusion criteria

Exclusion criteria: • Pre-stroke disability which interferes with the assessment of functional outcome at 90 days, i.e. mRS >2

Design outcomes

Primary

MeasureTime frame
The distribution of outcomes on the modified Rankin scale (mRS) at three months.

Secondary

MeasureTime frame
• Barthel Index • EQ5D5L • Adverse events

Contacts

Public ContactAyla van Ahee

Amsterdam UMC

a.e.vanahee@amsterdamumc.nl+31205666119

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)