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Completed

NCT Number: NCT04180436

Pharmacokinetics of Rivaroxaban After Bariatric Surgery

Data on pharmacokinetics of rivaroxaban after bariatric surgery and in morbid obesity are sparse. The aim of this study is to assess the pharmacokinetic and pharmacodynamic parameters of rivaroxaban, used at a therapeutic anticoagulant dose, in patients with previous bariatric surgery, with sleeve gastrectomy or gastric bypass, and in morbid obese subjects.

Four groups of 16 subjects per group are studied: Morbid obese subjects / Subjects who have undergone gastric bypass surgery / Subjects who have undergone sleeve gastrectomy surgery / Non-operated control subjects matched for age and BMI with operated subjects.

All patients (obese, surgical patients, and controls) will receive rivaroxaban 20mg once daily during 8 days. Blood samples will be taken predose (Baseline) and 0.5, 1, 2, 3, 6, 9, 12 and 24h post rivaroxaban administration at day1 and day8. PK and PD parameters will be compared between groups in order to explore the impact of bariatric surgery, type of surgery and body mass index on the pharmacological profile of rivaroxaban.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

CHRU de Brest

Brest, France, 29609

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Creatinine clearance measured by the Cockroft formula ≥ 60 mL / min
  • Patient meeting the specific criteria of one of the 4 groups:
  • morbidly obese patients with BMI ≥ 40
  • Patients operated by gastric bypass for over a year and with stable weight
  • Patients operated by sleeve gastrectomy for over a year and with stable weight
  • Control group: non-operated subjects but with an age and a BMI corresponding to those of the patients of the 2 operated groups.

Exclusion criteria

  • Indication for anticoagulant therapy, antiplatelet therapy or long-term nonsteroidal anti-inflammatory drugs
  • Clinically significant bleeding in progress
  • Taking oral or parenteral anticoagulants, or taking platelet antiaggregants within 4 weeks before inclusion
  • Congenital or acquired hemorrhagic disorders (eg von Willebrand disease, hemophilia)
  • Injury or disease, at significant risk of major bleeding (gastrointestinal ulceration, presence of malignant tumors with a high risk of bleeding, recent brain or spinal cord injury, recent cerebral, spinal or ophthalmic surgery, recent intracranial hemorrhage, known or suspected oesophageal varices , arteriovenous malformations, vascular aneurysms or major intraspinal or intracerebral vascular abnormalities)
  • Severe uncontrolled arterial hypertension
  • Active gastrointestinal disease potentially leading to bleeding disorders (esophagitis, gastritis, gastroesophageal reflux disease, chronic inflammatory bowel disease)
  • Vascular retinopathy
  • Bronchiectasis or history of pulmonary bleeding
  • Hypersensitivity to the active substance or to any of the excipients of rivaroxaban
  • Hepatic involvement associated with coagulopathy and clinically significant bleeding risk, including cirrhotic patients with Child Pugh Grade B or C score
  • Concomitant use of potent inhibitors or inducers of CYP3A4 and / or P-gp (azole antifungal or HIV protease inhibitor)
  • Participation in a paid and / or therapeutic study in the previous 3 months
  • Pregnant or lactating women,
  • Women of childbearing potential not using effective contraception

Treatment and study plan

rivaroxaban 20 mg once daily 8 days

Drug

Blood samples for the measurement of rivaroxaban PK parameters

Primary outcomes

  1. AUC of rivaroxaban

    Time frame: up to 8 days

    Rivaroxaban plasma concentrations was assessed by the reference method at the different sampling points to determine the area under the curve (AUC)

  2. Cmax of rivaroxaban

    Time frame: up to 8 days

    Cmax of rivaroxaban was assessed

  3. Tmax of rivaroxaban

    Time frame: up to 8 days

    Tmax of rivaroxaban was assessed

Secondary outcomes

  1. Prothrombin time

    Time frame: up to 8 days

    Prothrombin time of rivaroxaban was assessed

  2. Activated partial thromboplatin time (aPTT)

    Time frame: up to 8 days

    Activated partial thromboplatin time was assessed

  3. Fibrinogen levels

    Time frame: up to 8 days

    Fibrinogen levels was was assessed

  4. Rivaroxaban anti-Xa activity

    Time frame: up to 8 days

    Rivaroxaban anti-Xa activity was assessed

  5. Rate of bleedings

    Time frame: up to 15 days

    Treatment-Related Adverse Events were assessed

  6. Other adverse events

    Time frame: up to 15 days

    Number of other adverse events than bleedings was assessed

  7. Thrombin generation test of rivaroxaban

    Time frame: up to 8 days

    Thrombogram (thrombin generation test) data for each time analyzed allows measurement of peak height . These data will be used to model the PD of rivaroxaban and to estimate the PD variability.

  8. Thrombin generation test of rivaroxaban

    Time frame: up to 8 days

    Thrombogram (thrombin generation test) data for each time analyzed allows measurement of thrombin generation potential (FTE). These data will be used to model the PD of rivaroxaban and to estimate the PD variability.

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Collaborators

  • Bayer

Registry information

Official study title

Pharmacokinetics and Pharmacodynamics of rivAroxaban After Bariatric Surgery and in mORBid Obesity

Acronym: ABSORB

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Nov 27, 2019
Registry last updated
Dec 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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