Actively Recruiting

Phase 2
Age: 18Years - 100Years
All Genders
NCT01712620

Spironolactone for Pulmonary Arterial Hypertension

Led by National Institutes of Health Clinical Center (CC) · Updated on 2026-05-05

70

Participants Needed

1

Research Sites

676 weeks

Total Duration

On this page

Sponsors

N

National Institutes of Health Clinical Center (CC)

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Background: \- High blood pressure in the lungs, known as pulmonary arterial hypertension (PAH), is a rare disorder. In spite of recent advances in treatment, the death rate remains unacceptably high. Lung blood vessel function can be harmed by progressive injuries, such as inflammation, leading to worsening of the disease. A drug called spironolactone has been known to improve blood vessel function and reduce inflammation. Some people with PAH take spironolactone to help treat fluid retention. However, its effect on inflammation and blood vessel function in patients with PAH is not known. Researchers want to see if spironolactone can help these conditions in people with PAH. Objectives: \- To test the effectiveness of spironolactone in treating pulmonary arterial hypertension. Eligibility: \- Individuals at least 18 years of age with pulmonary arterial hypertension. Design: * This study will last for 24 weeks. Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected. * Participants will take either spironolactone or a placebo. They will take their study drug or placebo for 7 weeks. Treatment will be monitored with regular blood tests. * In Week 8, participants who have had no reaction to the treatment will receive a higher dose of the drug or placebo. * In Week 12, participants will have a study visit with heart and lung function tests. They will also have a 6-minute walk test, and provide blood and urine samples. * After additional study visits for blood samples, participants will have a final visit in Week 24. The tests from Week 12 will be repeated at this visit.

CONDITIONS

Official Title

Spironolactone for Pulmonary Arterial Hypertension

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 100 years with pulmonary arterial hypertension (WHO Group 1 PH)
  • On no medical therapy or stable PAH therapy for at least 4 weeks with no change in functional class
  • Hemodynamic confirmation by right heart catheterization: mean pulmonary artery pressure > 25 mmHg, pulmonary capillary wedge pressure ≤ 15 mmHg, pulmonary vascular resistance > 3 Wood units
  • Females able to become pregnant must agree to use effective contraception during the study
Not Eligible

You will not qualify if you...

  • Patients with right heart failure showing NYHA/WHO class IV symptoms and severe right ventricular dysfunction
  • History of cirrhosis with portal hypertension including ascites or hepatic encephalopathy
  • Active infection (except controlled HIV with low viral load)
  • Use of spironolactone or eplerenone within 30 days prior to enrollment
  • Known or suspected allergy to spironolactone
  • Pregnant or breastfeeding women
  • Age under 18 years
  • Unable to provide informed consent
  • Chronic kidney disease with eGFR < 35 mL/min/1.73m2
  • Serum potassium > 5 mEq/L at enrollment
  • Concurrent use of ACE inhibitors and angiotensin II receptor blockers at maximum doses
  • Use of drospirenone-containing oral contraceptives
  • Contraindications to MRI including implanted devices or inability to tolerate MRI
  • History of severe allergic reaction to gadolinium contrast
  • Chronic kidney disease with eGFR < 60 mL/min/1.73m2 for MRI studies only

AI-Screening

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Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

G

Grace M Graninger, R.N.

CONTACT

M

Michael A Solomon, M.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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