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Pharmacokinetics of rivaroxaban in elderly patients with non-valvular atrial fibrillation

Pharmacokinetics of rivaroxaban in elderly patients with non-valvular atrial fibrillation

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-15005948
Enrollment
Unknown
Registered
2015-01-19
Start date
2015-02-09
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

non-valvular atrial fibrillation

Interventions

A:rivaroxaban 15mg
B:rivaroxaban 15mg

Sponsors

Zhejiang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: age older than 65; BMI 18-24kg/m2; non-valvular atrial fibrillation.

Exclusion criteria

Exclusion criteria: Patients would be ineligible if they had received a therapeutic dose of low-molecular-weight heparin,or unfractionated heparin for more than 48 hours; or if they had any contrainidcation listed in the local labeling of enoxaparin, warfarin, or acenocoumarol. Other criteria for ineligiblity were another indication for vitamin K antagonist; a creatinine clearance below 30ml per minute; clinically significant liver disease or an alanine aminotransferase level that was more than three times the upper limit of the normal range; acitve bleeding or a high risk of bleeding contraindicating anticoagulant treatment; concomitant use of a strong inhibitor of cytochrome P-450 3A4 or a CYP3A4 inducer; participation in another experimental pharmacotherapeutic program within 30 days; or a life expectancy of less than 3 months.

Design outcomes

Primary

MeasureTime frame
plasma concentration of drug;

Countries

China

Contacts

Public ContactJing Yan
zjyylw@hotmail.com+86 0571 81595216

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026