A Phase 1 interventional study of Rivaroxaban 10 mg in Prophylaxis of Venous Thromboembolism, sponsored by Insel Gruppe AG, University Hospital Bern. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-04-11.
Sponsored by Insel Gruppe AG, University Hospital Bern · Phase 1, Interventional, and Prevention
Aim of this clinical Trial is the assessment of rivaroxaban PK/PD parameters in patients 6-8 months after bariatric surgery
Weight loss after bariatric surgery can putatively alter drug disposition of rivaroxaban. This may be due to an altered intestinal adaptations several months after the surgical procedure. The aim of this clinical trial is to investigate pharmacokinetic and pharmacodynamic parameters after single application of 10 mg rivaroxaban in patients with prior bariatric intervention (Roux-en-y-gastric bypass or sleeve gastrectomy 6-8 months ago). PK/PD parameters will be assessed during 12 hours after application of rivaroxaban.
818 studies on the registry are indexed under Thromboembolism; 98 are open to participants now.
This study's enrollment of 13 is below the median of 196 across 436 interventional studies indexed under Thromboembolism.
Browse Thromboembolism studies →Insel Gruppe AG, University Hospital Bern is the lead sponsor of 724 studies on the registry; 177 are open to participants now.
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Exclusion Criteria:
Drug: Rivaroxaban 10 mg
At study month 7 (+/-1 month), patients receive at 8 a.m. a single dose of 10 mg rivaroxaban. Study specific blood tubes are sampled the same day at the indicated time points from T -1h to T 12h.
AUC of rivaroxaban
Time frame: 1 year
Cmax of rivaroxaban
Time frame: 1 year
Tmax of rivaroxaban
Time frame: 1 year
Prothrombin time (PT)
Time frame: 1 year
Activated partial thromboplastin time (aPTT)
Time frame: 1 year
Levels of Prothrombin fragment (F1+F2)
Time frame: 1 year
Levels of Thrombin-antithrombin-complexes (TAT)
Time frame: 1 year
Levels of D-Dimers
Time frame: 1 year
Plan to share: No
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This study is completed, as verified in Apr 2017. You cannot join it, but the record below documents what was studied.
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Insel Gruppe AG, University Hospital Bern