Phase 3
N=61
Mineralocorticoid Antagonism and Endothelial Dysfunction in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
ADPKD
Bottom Line
View on ClinicalTrials.gov: NCT01853553 ↗Enrolled (actual)
61
Serious AEs
0.0%
Results posted
Aug 2019
Primary outcome: Primary: Change From Baseline in Flow Mediated Dilation at 6 Months. — -0.2; -0.4 Percent change.
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Spironolactone (Drug); Sugar pill (Drug)
- Age
- Adult · 20+ yrs
- Sex
- All
- Sponsor
- University of Colorado, Denver
- Primary completion
- Jan 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Flow Mediated Dilation at 6 Months. |
-0.2; -0.4 | — |
| SECONDARY Change From Baseline in Vascular Stiffness at 6 Months. |
-37; -1 | — |
Summary
The proposed research will determine the effectiveness of blocking aldosterone for improving the health and function of arteries in patients with autosomal dominant polycystic kidney disease (ADPKD). The study also will provide insight into how blocking aldosterone improves artery health by determining the physiological mechanisms (biological reasons) involved. Overall, the proposed research will provide important new scientific evidence upon which physicians can base recommendations to patients with ADPKD to decrease risk of developing cardiovascular diseases.
Eligibility Criteria
Inclusion Criteria
- Aged 20-55 years;
- Adults with ADPKD diagnosis based on Ravine criteria aged ≥ 30 years
- Estimated glomerular filtration rate ≥ 60 ml/min/1.73m2
- Hypertension defined as a systolic BP > 130 mm Hg and/or diastolic BP > 80 mmHg based on 3 separate measurements within the past year and currently on a minimum dose of an angiotensin converting enzyme inhibitor (minimum dose 10 mg P.O qd) or angiotensin receptor blocker (i.e., Losartan 25 mg P.O qd)
- If using antioxidants and/or omega-3 fatty acids, must discontinue 4 weeks prior to participation
- Free from alcohol dependence or abuse
- Mini-mental state examination score ≥ 24; ability to provide informed consent
- BMI 5.5 millequivalents or any single serum potassium > 6.0 millequivalents within the previous 6 months
- Receiving an aldosterone antagonist within the previous 6 months
- Use of a potassium sparing diuretic or any other drug that could contribute to hyperkalemia
- Uncontrolled hypertension
- Current smokers or history of smoking in the past 12 months
- History of liver disease
- History of heart failure (EF < 35%)
- History of hospitalizations within the last 3 months
- Active infection or antibiotic therapy
- Warfarin use
- Immunosuppressive therapy within the last year
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT01853553). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.