CHRU de Brest
Brest, France, 29609
NCT Number: NCT04180436
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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Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Brest, France, 29609
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Blood samples for the measurement of rivaroxaban PK parameters
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)
Time frame: up to 8 days
Cmax of rivaroxaban was assessed
Time frame: up to 8 days
Tmax of rivaroxaban was assessed
Time frame: up to 8 days
Prothrombin time of rivaroxaban was assessed
Time frame: up to 8 days
Activated partial thromboplatin time was assessed
Time frame: up to 8 days
Fibrinogen levels was was assessed
Time frame: up to 8 days
Rivaroxaban anti-Xa activity was assessed
Time frame: up to 15 days
Treatment-Related Adverse Events were assessed
Time frame: up to 15 days
Number of other adverse events than bleedings was assessed
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.
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.
University Hospital, Brest
Other
Pharmacokinetics and Pharmacodynamics of rivAroxaban After Bariatric Surgery and in mORBid Obesity
Acronym: ABSORB
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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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