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NCT06691230: PROPHET

PeRfusiOn Post tHrombEcTomy (PROPHET)

Recruiting now Last updated 15 November 2024
What this trial tests

trial in Stroke, Acute, Ischemic in 279 participants. Currently enrolling.

Timeline
1 November 2024
Primary endpoint
30 November 2027
28 February 2028

Quick facts

Lead sponsorInsel Gruppe AG, University Hospital Bern
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment279
Start date1 November 2024
Primary completion30 November 2027
Estimated completion28 February 2028
Sites2 locations across Switzerland

Conditions studied

Sponsor

Insel Gruppe AG, University Hospital Bern

Who can join

18 and older, any sex, with Stroke, Acute, Ischemic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Endovascular mechanical thrombectomy is the standard of care for treating patients with a large-vessel occlusion acute ischemic stroke. However, in more than half of these patients, remaining distal vessel occlusions limit the benefit of this therapy. Currently the detection of residual vessel occlusions and the decision for further treatment by the operator is based on the 2D digital subtraction angiography (DSA) images. However, this technique has several limitations. Recently, a new imaging technique, with the possibility to acquire 3D time-resolved perfusion images directly in the operating room was introduced (the flat-panel detector computed tomography perfusion imaging, FDCTP). It can overcome the spatial limitations of 2D DSA, but the details on clinical validation and utility of FDCTP are currently lacking.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Insel Gruppe AG, University Hospital Bern trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06691230.

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