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CompletedNCT02832947Updated Apr 11, 2017

PK of Rivaroxaban in Bariatric Patients - Extension

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

Phase
Phase 1
Study type
Interventional
Enrollment
13
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

Aim of this clinical Trial is the assessment of rivaroxaban PK/PD parameters in patients 6-8 months after bariatric surgery

Read the detailed description

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.

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Conditions studied

  • Prophylaxis of Venous Thromboembolism
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In context

Thromboembolism

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 →

Lead sponsor

Insel Gruppe AG, University Hospital Bern is the lead sponsor of 724 studies on the registry; 177 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient with past elective bariatric surgery (Roux-en-Y gastric bypass surgery or sleeve gastrectomy 6-8 months ago)
  • Patient aged 18 years and older
  • BMI ≥ 35 kg/m2
  • Women of child-bearing age: Willingness of using a double barrier contraception method during the study
  • Written, informed consent

Exclusion criteria

Exclusion Criteria:

  • Intake of oral anticoagulants (phenprocoumon, acenocoumarol, dabigatran, etexilate, apixaban etc.) 4 weeks prior to inclusion in the study
  • Application of parenteral anticoagulants (unfractionated heparin, low molecular weight heparins, heparin derivates (fondaparinux etc.) 4 weeks prior to inclusion in the study
  • Pharmacologic platelet inhibition 4 weeks prior to inclusion in the study
  • Known coagulation disorders (e.g. Willebrand's disease, haemophilia)
  • Evidence for deep vein thrombosis or pulmonary embolism in the personal history or in the history of first degree relatives
  • Medical condition that is associated with an increased risk for VTE, i.e. active cancer disease, lupus erythematodes chronic inflammatory bowel disease
  • Active, clinically significant bleeding
  • Congenital or acquired bleeding disorder
  • Uncontrolled severe hypertension
  • Active gastrointestinal disease that can potentially lead to bleeding disorder: oesophagitis, gastritis, gastroesophageal reflux disease, chronic inflammatory bowel disease
  • Vascular retinopathy
  • Bronchiectasis or history of pulmonary bleeding
  • Prior stroke or TIA
  • Hereditary galactose intolerance, Lapp lactase deficiency, glucose-lactose malabsorption
  • Severe renal impairment with a creatinine clearance (GFR) of \< 30ml/min
  • Positive pregnancy test, pregnancy or nursing women
  • High risk of bleeding (e.g. active ulcerative gastrointestinal disease)
  • Known intolerance of the study medication rivaroxaban
  • Concomitant treatment with strong CYP3A4 inhibitors (e.g. ketoconazole, itraconazole, lopinavir, ritonavir, indinavir)
  • Concomitant treatment with an P-glycoprotein inhibitor and weak or moderate CYP3A4 inhibitor (e.g. erythromycin, azithromycin, diltiazem, verapamil, quinidine, ranolazine, dronedarone, amiodarone, felodipine)
05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
13 participants (actual)

Study arms

  • Other
    Rivaroxaban Arm

    Drug: Rivaroxaban 10 mg

Interventions

  • DrugRivaroxaban 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.

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What researchers measure

Primary outcomes

  1. AUC of rivaroxaban

    Time frame: 1 year

  2. Cmax of rivaroxaban

    Time frame: 1 year

  3. Tmax of rivaroxaban

    Time frame: 1 year

  4. Prothrombin time (PT)

    Time frame: 1 year

  5. Activated partial thromboplastin time (aPTT)

    Time frame: 1 year

  6. Levels of Prothrombin fragment (F1+F2)

    Time frame: 1 year

  7. Levels of Thrombin-antithrombin-complexes (TAT)

    Time frame: 1 year

  8. Levels of D-Dimers

    Time frame: 1 year

07

Study locations

1 site
  • University Hospital, Inselspital Berne
    Berne, 3010, Switzerland
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02832947
Lead sponsor
Insel Gruppe AG, University Hospital Bern
Collaborators
University of Lausanne Hospitals
Responsible party
Sponsor
First posted
Jul 14, 2016
Start date
Feb 2016
Primary completion
Jun 2016
Completion
Oct 2016
Last update
Apr 11, 2017

Study contacts

Dino Kröll, MD
study chair · Insel Gruppe AG, University Hospital Bern

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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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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