Trials / Completed
CompletedNCT06997952
Febuxostat Effect on Chronic Kidney Disease Progression And Carotid Intima-Media Thickness
Impact of Febuxostat on Disease Progression and Carotid Intima-Media Thickness in Patients With Chronic Kidney Disease
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Ain Shams University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to evaluate the impact of febuxostat on both carotid intima-media thickness and disease progression in individuals with chronic kidney disease
Detailed description
For all participants, comprehensive data collection was performed, encompassing detailed medical histories including patients' clinical and demographic characteristics (age, gender, BMI, associated comorbidities as HTN, and DM, etiology of CKD.) Laboratory investigations were conducted at baseline and after a three-month follow-up period. These investigations included: serum uric acid., creatinine, blood urea nitrogen, calcium, phosphorus., albumin., magnesium, intact parathyroid hormone (iPTH), lipid profile (cholesterol, triglycerides, LDL, HDL), urine protein to creatinine ratio. Radiological investigations: Carotid artery duplex (medial wall thickness) was also conducted at baseline and after a three-month follow-up period. Thickening of the artery wall is a hallmark of atherosclerosis and vascular calcification.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Febuxostat 40 mg | Febuxostat will be given daily for 12 weeks The prescribed dosage was 40 mg taken once daily, self-administered by the patients in addition to their standard treatment. |
Timeline
- Start date
- 2024-05-24
- Primary completion
- 2024-08-24
- Completion
- 2024-08-24
- First posted
- 2025-05-31
- Last updated
- 2025-05-31
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06997952. Inclusion in this directory is not an endorsement.