MedPath

Targeting Leukotrienes in Kidney Disease

Phase 3
Terminated
Conditions
Diabetic Kidney Disease
Interventions
Registration Number
NCT05362474
Lead Sponsor
University of Colorado, Denver
Brief Summary

Diabetic kidney disease (DKD) is associated with significant morbidity and mortality. Identifying new treatments for DKD to be used alone or in combination with other therapies is a high priority. Inflammation plays a key role in DKD and targeting pro-inflammatory lipid mediators called leukotrienes may represent a promising therapy for DKD. The current proposal will investigate whether montelukast, a leukotriene antagonist, reduces proteinuria and improves vascular function and arterial stiffness in patients with DKD.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
5
Inclusion Criteria
  • CKD stage 3
  • urine albumin to creatinine ratio 200-5000 mg/g
  • blood pressure <140/90 mmHg
  • use of angiotensin converting enzyme inhibitor or angiotensin receptor blocker with stable dose for 4 weeks
  • history of diabetes type 1 or 2
  • BMI <40 kg/m2
  • Stable antihypertensive regimen for at least one month prior to enrollment
  • Stable diabetes regimen for at least one month prior to enrollment
  • Sedentary or recreationally active (<2 days of vigorous aerobic exercise as vigorous exercise may affect vascular function measurements)
  • Able to provide consent
Exclusion Criteria
  • Significant comorbid conditions that lead the investigator to conclude that life expectancy is less than 1 year
  • Uncontrolled hypertension
  • Factors judged to limit adherence to interventions (e.g. history of medication noncompliance, noncompliance with follow up visits, significant cognitive impairment, etc.)
  • Anticipated initiation of dialysis or kidney transplantation within 3 months
  • Current participation in another research study
  • Pregnancy or planning to become pregnant or currently breastfeeding
  • Allergy to aspirin
  • Severe hepatic impairment (Child-Pugh Class C)
  • History of major psychiatric disorder
  • Use of inhaled or systemic corticosteroids or long-acting beta agonists (higher risk of neuropsychiatric reaction)
  • Current use of SGLT2 inhibitor
  • Current use of phenobarbital, rifampin or carbamazepine.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
montelukastMontelukastmontelukast 10mg orally once a day
Primary Outcome Measures
NameTimeMethod
Change in Albuminuria at 3 monthsBaseline, 3 months

Change in 24-hour urine albumin excretion at 3 months

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Colorado

🇺🇸

Aurora, Colorado, United States

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