Maintenance of an Antiaggregation by Acetylsalicylic Acid, While a Extracorporeal Lithotripsy Session on a Kidney Stone is Perfomed: Comparative Unicentric Prospective Study
Launched by UNIVERSITY HOSPITAL, CLERMONT-FERRAND · Feb 12, 2018
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating whether patients who are taking a low dose of aspirin (250 mg or less) can safely continue their medication during a specific treatment for kidney stones called extracorporeal lithotripsy (ECL). ECL is a procedure that uses shock waves to break up kidney stones into smaller pieces so they can be more easily passed. The study aims to see if continuing aspirin might lead to fewer complications, like bleeding or hematomas (bruises) around the kidneys, while still effectively treating the stones.
To participate in this trial, individuals must be over 18 years old and have at least one kidney stone that requires ECL treatment. They must also be taking a specific type of aspirin called Kardégic 75. Potential participants should not have any bleeding disorders, be on other blood-thinning medications, or have any other conditions that would prevent safe participation in the ECL procedure. If eligible, participants can expect to receive the ECL treatment while continuing their aspirin, and they will be monitored for any side effects or complications related to the procedure. This study is important as it could help simplify treatment for patients who need to manage both kidney stones and cardiovascular health.
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- • Over 18 yo patients
- • Patients with 1 renal lithiasis (at least) requiring treatment with extracorporeal lithotripsy
- • Patients taking Kardégic 75 (monotherapy
- Exclusion Criteria:
- • Patients with known (or previously known) bleeding disorders on the pre-treatment assessment
- • Patients with anticoagulant therapy or other anti-aggregating therapy (eg Kardegic at 75mg, AVK, NACO, LMWH, HNF, P2Y12 inhibitor)
- • Patients with another contrindication to the ECL.
- • Patients with prescription of more than the outset 1 ECL session
- • Tutelage, curatorship, justice safeguarding, deprived of liberties, unaffiliated SS, impaired comprehension abilities, pregnant and lactating women.
About University Hospital, Clermont Ferrand
The University Hospital of Clermont-Ferrand is a leading academic medical institution dedicated to advancing healthcare through innovative research and clinical trials. Renowned for its multidisciplinary approach, the hospital integrates cutting-edge scientific inquiry with patient care, fostering an environment that promotes collaboration among healthcare professionals, researchers, and academic partners. With a strong commitment to improving patient outcomes, the institution actively engages in a wide array of clinical studies, ranging from early-phase trials to large-scale interventions, aimed at addressing critical health challenges and enhancing treatment modalities. Its state-of-the-art facilities and expertise make it a pivotal contributor to clinical research in the region and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Clermont Ferrand, , France
Patients applied
Trial Officials
Marlène GUANDALINO, MD
Study Director
University Hospital, Clermont-Ferrand
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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