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Study identifier: NCT07003646 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Reperfusion Treatment in Acute Pulmonary Embolism

Condition: Pulmonary Embolism  ·  Sponsor: Sahlgrenska University Hospital

PhaseN/A
Planned participants220
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

International guidelines recommend immediate reperfusion with systemic thrombolysis (ST) as first-line treatment in high-risk pulmonary embolism (PE). The therapy improves hemodynamics and overall survival but is also associated with a significant risk of severe bleeding. Catheter-directed intervention (CDI) is recommended as an alternative reperfusion therapy in high-risk PE when ST is contraindicated or has failed, as well as in patients who deteriorate or fail to improve during anticoagulation (AC) treatment. Despite lack of high-quality evidence and randomized studies between CDI and standard care, the use of CDI is spreading rapidly in high-risk PE and in less severe PE not fulfilling current treatment criteria.

This description comes directly from the study's public registry record.

Talk to the study team

Freyr Einarsson, MD  ·  +46500 43 10 36  ·  freyr.einarsson@vgregion.se

Annika Odenstedt, coordinator  ·  +46 343 53 94  ·  annika.odenstedt@vgregion.se

Always discuss trial participation with your own doctor first.

Locations (13)

Aarhus University HospitalAarhus, DenmarkRecruiting
RigshospitaletCopenhagen, DenmarkRecruiting
Odense University HospitalOdense, DenmarkRecruiting
Sahlgrenska University HospitalGothenburg, SwedenRecruiting
Linköping University HospitalLinköping, SwedenRecruiting
Sunderby HospitalLuleå, SwedenRecruiting
Skåne University HospitalLund, SwedenRecruiting
Örebro University HospitalÖrebro, SwedenRecruiting
Danderyd HospitalStockholm, SwedenRecruiting
Karolinska University Hospital HuddingeStockholm, SwedenRecruiting
Karolinska University Hospital SolnaStockholm, SwedenRecruiting
SödersjukhusetStockholm, SwedenRecruiting

+ 1 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07003646