Clinical Surveillance vs. Anticoagulation for Low-risk Patients With Isolated Subsegmental Pulmonary Embolism: a Multicenter Randomized Placebo-controlled Non-inferiority Trial

Who is this study for? Adult patients with isolated subsegmental pulmonary embolism
What treatments are being studied? Rivaroxaban
Status: Recruiting
Location: See all (39) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The clinical significance of pulmonary embolism (PE) limited to the subsegmental pulmonary arteries, so called isolated subsegmental pulmonary embolism (SSPE), remains controversial. Whether isolated SSPE represents true PE, a clinically more benign form of PE, a physiologic lung clearing process, or a false positive result (artifact) is currently unclear and hence, whether patients with isolated SSPE benefit from anticoagulant treatment is uncertain. Despite growing evidence from observational studies that withholding anticoagulation may be a safe option in selected patients with isolated SSPE (i.e., those without concomitant deep vein thrombosis, cancer, etc.), most patients with isolated SSPE receive anticoagulant treatment, which is associated with an increased risk of bleeding. The overall objective of the randomized controlled SAFE-SSPE trial is to evaluate the efficacy and safety of clinical surveillance without anticoagulation compared to anticoagulation treatment in low-risk patients with isolated SSPE.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed Consent as documented by signature

• Age ≥18 years

• Objective diagnosis of symptomatic or asymptomatic isolated SSPE

Locations
Other Locations
Belgium
Centre hospitalier universitaire de Liege
NOT_YET_RECRUITING
Liège
Cliniques Universitaires Saint-Luc
RECRUITING
Woluwe-saint-lambert
Canada
The Ottawa Hospital
RECRUITING
Ottawa
France
Centre Hospitalier Regional Et Universitaire De Brest
RECRUITING
Brest
CHU Gabriel-Montpied
RECRUITING
Clermont-ferrand
Centre Hospitalier Universitaire De Dijon
RECRUITING
Dijon
Hôpital Bicêtre - APHP
RECRUITING
Le Kremlin-bicêtre
Hospital Edouard Herriot
RECRUITING
Lyon
CHU De Rouen
RECRUITING
Rouen
CHU ST Etienne - Hôpital Nord
RECRUITING
Saint-priest-en-jarez
Netherlands
Albert Schweitzer Ziekenhuis Dordrecht
RECRUITING
Dordrecht
Medisch Spectrum Twente
RECRUITING
Enschede
Leiden University Medical Center
RECRUITING
Leiden
Erasmus Universitair Medisch Centrum
RECRUITING
Rotterdam
Haaglanden Medisch Centrum
WITHDRAWN
The Hague
Isala Klinieken Zwolle
RECRUITING
Zwolle
Switzerland
Cantonal Hospital of Aarau
RECRUITING
Aarau
Cantonal Hospital of Uri
WITHDRAWN
Altdorf
Cantonal Hospital of Baden
RECRUITING
Baden
University Hospital of Basel
RECRUITING
Basel
Tiefenau Hospital
COMPLETED
Bern
University Hospital Inselspital
RECRUITING
Bern
Hospital of Bienne
RECRUITING
Biel/bienne
Regional Hospital of Emmental
RECRUITING
Burgdorf
Hospital of Delémont
RECRUITING
Delémont
Cantonal Hospital of Frauenfeld
RECRUITING
Frauenfeld
Cantonal Hospital of Fribourg
RECRUITING
Fribourg
Geneva University Hospital
RECRUITING
Geneva
University Hospital of Lausanne
RECRUITING
Lausanne
Cantonal Hospital of Liestal
RECRUITING
Liestal
Cantonal Hospital of Lucerne
WITHDRAWN
Lucerne
Hospital of Neuchâtel
RECRUITING
Neuchâtel
Hospital of Nyon
WITHDRAWN
Nyon
Cantonal Hospital of Olten
WITHDRAWN
Olten
Cantonal Hospital of St. Gallen
RECRUITING
Sankt Gallen
Hospital of Sion
WITHDRAWN
Sion
Cantonal Hospital of Winterthur
RECRUITING
Winterthur
Triemli Hospital
RECRUITING
Zurich
University Hospital Zürich
RECRUITING
Zurich
Contact Information
Primary
Drahomir Aujesky, Prof. MD MSc
SAFE-SSPE@insel.ch
+41 31 632 88 84
Backup
Tobias Tritschler, Dr. MD MSc
SAFE-SSPE@insel.ch
+41 31 63 2 01 46
Time Frame
Start Date: 2020-05-15
Estimated Completion Date: 2026-05
Participants
Target number of participants: 276
Treatments
Active_comparator: Anticoagulation
Patients in the anticoagulation group will receive rivaroxaban 15 mg twice daily for the first 21 days, followed by 20 mg once daily for an overall treatment duration of 90 days.
Placebo_comparator: No anticoagulation
Patients in the group without anticoagulation will receive placebo twice daily for the first 21 days, followed by one tablet daily for an overall treatment duration of 90 days.
Sponsors
Leads: Drahomir Aujesky
Collaborators: Bayer, The Ottawa Hospital, Schweizerischer Nationalfonds, University of Bern, Leiden University Medical Center

This content was sourced from clinicaltrials.gov

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