NCT06998862Toboroz3. fázis
Colchicine in Chronic Kidney Disease Patients
Efficacy of Colchicine in Secondary Prevention of Vascular Events and Renal Progression in Patients With Moderate Chronic Kidney Disease
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. máj. 31. · Több mint 12 hónapja nem frissült - kérdezd meg a helyszínt, nyitott-e még
Rövid összefoglaló (regiszter, angolul)
The ColchiRen study is a phase 3, controlled, prospective, randomized, double-blind, and multicenter clinical trial. Its main objective is to demonstrate the benefit of low-dose colchicine treatment in secondary prevention of cardiovascular events in patients with moderate CKD. As a secondary objective, it aims to explore the potential beneficial anti-inflammatory effect on the progression of CKD.
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 3. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 744 (tervezett)
- Első benyújtás
- 2025. máj. 4.
- Kezdés
- 2025. febr. 12.
- Elsődleges befejezés
- 2028. dec. 30.
- Fő szponzor
- Hospital General Universitario Gregorio Marañon
- Betegségek
- Krónikus vesebetegség
- NCT-szám
- NCT06998862
- EU CT-szám
- 2023-505868-11-00
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 3. fázis
- Tervezett résztvevők: 744
- 2025. febr. 12. és az elsődleges befejezés (2028. dec. 30.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
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Korábbi kezelés
- Current treatment with colchicine, or within the month prior to inclusion.
- Hospital admission for any cause within the 3 months prior to study inclusion.
- Immunosuppressive treatment within the 12 weeks prior to study inclusion.
- Chronic treatment with non-steroidal anti-inflammatory drugs (NSAIDs).
- Pregnancy and breastfeeding at the time of inclusion. Contraceptive methods are required for women of reproductive age. Women with no capacity for pregnancy are considered to be those with:
- History of hysterectomy, bilateral salpingectomy, bilateral oophorectomy, or bilateral tubal ligation.
- Documented infertility. Postmenopausal women, defined as amenorrhea for more than 12 months without other medical cause. In case of doubt, confirmation with elevated follicle-stimulating hormone (FSH) levels is recommended.
- Women of reproductive capacity must use a method of contraception with proven effectiveness until 8 weeks after the end of the study. Acceptable methods include:
- Intrauterine device (IUD) placement at least 6 weeks before study inclusion. Hormonal contraception with progestogens only, associated with ovulation inhibition: oral, injectable, or implantable, at least 6 weeks before study inclusion.
- Progestin-releasing intrauterine system (IUS) at least 6 weeks before study inclusion.
- Combined hormonal contraception (containing estrogen and progestogens) associated with ovulation inhibition: oral, intravaginal, transdermal, at least 6 weeks before study inclusion.
- Other contraceptive methods (sexual abstinence, barrier methods, spermicides, etc.) are not considered acceptable for participation in this study
- thrombocytopenia <50,000 cells/μL during the month prior to inclusion
- Neutropenia defined as <1500 cells/mcL during the month prior to inclusion.
- Treatment with CYP3A4 inhibitors and/or P-glycoprotein inhibitors (antivirals, azole antifungals, aminoglycosides, cyclosporine) in the month prior to their inclusion in the study.
Más betegség
- Active malignant neoplasm (except non-melanoma skin cancer or carcinoma in situ). Patients with a history of malignant neoplasm who have remained disease-free for the past 3 years may be included.
- Uncontrolled or symptomatic chronic inflammatory disease (rheumatoid arthritis, systemic lupus erythematosus, Crohn's disease, ulcerative colitis, etc.).
- Active infection with hepatitis B virus, hepatitis C virus, or human immunodeficiency virus.
- Poorly controlled hypertension (>160/90 mmHg) at the time of inclusion.
- Gastric ulcer
- History of aplastic anemia diagnosed through bone marrow biopsy.
Laborértékek
- History of allergy or intolerance to colchicine or any of its excipients (dihydrate calcium hydrogen phosphate, microcrystalline cellulose, anhydrous colloidal silica, magnesium stearate).
- Anemia defined as hemoglobin <10.5 g/dL during the month prior to inclusion.
Egyéb
- Liver cirrhosis of any cause, grade B or C according to Child-Pugh.
Kiket keres a vizsgálat
- Age between 18 and 99 years. Moderate chronic kidney disease, defined as an estimated glomerular filtration rate (eGFR) by the CKD-EPI formula between 30 and 59 mL/min/1.73 m².
- History of a previous cardiovascular event:
- Acute coronary syndrome. Admission for angina pectoris. Transient ischemic attack or non-cardioembolic ischemic stroke. Coronary revascularization. Peripheral vasculopathy, defined as: embolism or acute peripheral arterial ischemia, or the need for amputation or surgical revascularization.
- Finding of coronary artery disease on imaging test.
Életkor a regiszterben: 18 év – 99 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Hospital General Universitario Gregorio Marañón | Madrid | Spanyolország | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.