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Clinical Trials in Denmark / NCT04330729
Recruiting Not applicable

The Effect of Salicylate on Platelet Function in CKD (Chronic Kidney Disease) Patients Treated With Aranesp

NCT04330729 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2020-04-15
Last updated
2024-01-25

Condition(s) studied

Erythropoietin Adverse Reaction

Investigational drug(s) / intervention(s)

Acetylsalicylic acid →

Acetylsalicylic acid: Se arm description

Study summary

The aim of the study is to

1. To determine whether treatment with Erythropoiesis-stimulating agents (in the form of Aranesp®) affects platelet function, and how.
2. To determine whether salicylate treatment changes the effect of EPO (erythropoietin) on platelet function.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * Chronic hemodialysis, peritoneal dialysis or CKD 5 treated conservatively * aged 18-85 * indication for treatment with Erythropoiesis-stimulating agents (ESA) Exclusion Criteria: 1. Known allergy to ASA 2. Known contraindication to ASA, e.g. recent bleeding episode. 3. Known indication for ASA. If the patient is being treated with ASA, and the physician does not find any indication for this treatment, this can be stopped, and the patient included after 4 weeks. 4. Raised reticulocyte count 5. Current anticoagulant therapy, e.g. warfarin, ADP receptor inhibitor (excepting short-term anticoagulant therapy in connection with dialysis) 6. Short expected length of life 7. Inability to give informed consent 8. Expected non-compliance 9. Active cancer - except for non-melanoma skin-cancer 10. Iron deficiency (defined as a reticulocyte Hgb \<1,8 fmol. Patients can be included when their iron deficiency has been cured. . 11. Change in ESA dosis \>33,3% within previous 2 month 12. Fertile women. Pregnancy is excessively rare in dialysis patients. Women who are \<50 years, or who are still menstruating will be excluded from the study. 13. Stable Aranesp ® dose \<20 µg/week.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Medicinsk afdeling, SUH Roskilde Roskilde Denmark Recruiting

More Zealand University Hospital trials in Denmark

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04330729 on ClinicalTrials.gov ↗ ← All trials in Denmark