Clinical Trial Details
Trial ID: | L0117 |
Source ID: | NCT04006093 |
Associated Drug: | Apixaban Oral |
Title: | Apixaban in Subjects With Peritoneal Dialysis |
Acronym: | ApiDP |
Status: | COMPLETED |
Study Results: | NO |
Results: | |
Conditions: | Chronic Renal Insufficiency|Peritoneal Dialysis |
Interventions: | DRUG: Apixaban Oral |
Outcome Measures: | Primary: Apixaban area Under the curve, Measurement of apixaban plasma concentrations at different times., Day 3|Apixaban maximum plasma concentration, Measurement of apixaban plasma concentrations at different times., Day 3 | Secondary: anti-Xa activity, anti-Xa activity plasma measurements, Hour 0, Hour 3, Hour 9 and Hour 72|TP activity, TP activity plasma measurements, Hour 0, Hour 3, Hour 9 and Hour 72|TCA activity, TCA activity plasma measurements, Hour 0, Hour 3, Hour 9 and Hour 72|Apixaban urinary elimination, Measurement of apixaban urinary concentrations, Day 3|Apixaban maximum peritoneal concentration, Measurement of apixaban peritoneal fluid concentrations, day 3 |
Sponsor/Collaborators: | Sponsor: University Hospital, Caen | Collaborators: University Hospital, Rouen |
Gender: | ALL |
Age: | ADULT, OLDER_ADULT |
Phases: | PHASE1 |
Enrollment: | 24 |
Study Type: | INTERVENTIONAL |
Study Designs: | Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: OTHER |
Start Date: | 2019-12-08 |
Completion Date: | 2022-12-10 |
Results First Posted: | |
Last Update Posted: | 2023-01-20 |
Locations: | CHU Caen, Caen, 14000, France |
URL: | https://clinicaltrials.gov/show/NCT04006093 |