Spironolactone for Pulmonary Arterial Hypertension

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-100
SponsorNational Institutes of Health Clinical Center (CC)

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

mean pulmonary artery pressure of > 25 mmHg at rest,

pulmonary capillary wedge pressure of <= 15 mmHg (or a left ventricular end-diastolic pressure of <= 12 mmHg) and

pulmonary vascular resistance of > 3 Wood units (240 dyn.s.cm^-5).

Disqualifiers

NYHA/WHO class IV symptoms

Echocardiographic evidence of severe RV dysfunction

Clinical evidence of right heart failure which may include, but is not limited to elevated jugular venous pressure, ascites, and lower extremity edema

Patients with WHO Group 1 pulmonary hypertension and a prior diagnosis of cirrhosis with portal hypertension as evidenced by a history of ascites, hepatic encephalopathy and/or varices prior to enrollment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Spironolactone

    Drug

    Initial dose, 25 mg (pink capsule) orally, daily. If well tolerated at 7-9 wks then increased to 50 mg (brown capsule) daily.

  • Placebo

    Drug

    Initial dose, pink sugar capsule, daily. If well tolerated at 7-9 wks then changed to brown sugar capsule, daily.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Group AExperimental treatment 1 intervention
Group B: Group BPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in placebo corrected 6-minute walk distance

Change in placebo corrected 6-minute walk distance.

Time frame
6 months

Secondary outcomes

1

Change in placebo corrected VO2 max

Time frame
6 months
2

Change in right ventricular function

Time frame
6 months
3

Biomarkers of vascular inflammation

Time frame
6 months
4

Rate of study drug discontinuation due to hyperkalemia, renal insufficiency, or other side effects such as breast pain and gynecomastia

Time frame
6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

National Institutes of Health Clinical Center (CC)

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator

University of Pennsylvania

Collaborator

University of Maryland, Baltimore

Collaborator

Medstar Health Research Institute

Collaborator

New England Medical Center, Tufts University School of Medicine

Collaborator