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Insulin Resistance in Pulmonary Arterial Hypertension

Primary Purpose

Hypertension, Pulmonary

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
bosentan
Pioglitazone
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension, Pulmonary focused on measuring pulmonary hypertension & insulin resistance

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients with Pulmonary Arterial Hypertension (PAH) must be stable on therapy for at least 3 months prior to enrollment in the trial. We will include patients with idiopathic PAH and Familial PAH as well as PAH associated with collagen vascular disease or drug or toxin exposure. With the exception of PAH, subjects must be free of major medical illnesses, including diabetes mellitus (must have fasting plasma glucose < 126 mg/dL and taking no anti-hyperglycemic agent), malignancy or significant hepatic or renal disease. Subjects may be hypertensive and on anti-hypertensive medications as long as blood pressure is < 150/100 mm Hg. Subjects may also be dyslipidemic and/or taking drugs to improve abnormalities of lipid metabolism, but they will be excluded if they are taking medications known to alter insulin sensitivity, including glucocorticoids, niacin, anti-retrovirals, thiazolidinediones, or metformin. Use of oral contraceptives or estrogen and/or progesterone replacement therapy is permitted. Weight must be stable and the subjects agree not to change their eating habits or exercise regimen during the study period. There will be no restrictions with regard to race or socioeconomic status, and the racial/ethnic composition of the study population will be reflective of the communities surrounding the Stanford University Medical Center.

Exclusion Criteria:

* Vulnerable subject status.

  • Concurrent Endothelin-1 antagonist therapy
  • Concurrent Thiazolidinedione therapy
  • New York Heart Class III or IV
  • PAH related to other etiologies.
  • Diabetes Mellitus with Fasting Glucose Levels > 126 mg/dL
  • Allergy or hypersensitivity to pioglitazone or bosentan administration.
  • Current treatment with statin therapy.
  • Initiation of PAH therapy (prostacyclin analogues, phosphodiesterase-5 inhibitors) within three months of enrollment.
  • Inability or unwillingness to avoid systemic steroid containing medications for four months. Inhaled steroid use is acceptable.
  • Current or recent use or planned treatment with: glyburide, cyclosporine, nilotinib, nisoldipine, ranolazine, thioridazine
  • Hepatic transaminases > 2x the upper limit of normal at the center at screening.
  • Current or recent (< 6 months) chronic heavy alcohol consumption.
  • Current use of another investigational drug (non-FDA approved) for PAH.
  • Lung transplant recipients.
  • History of myositis.
  • Renal failure (Cr 2.0).
  • Hospitalized or acutely ill.
  • Chronic liver disease (cirrhosis, chronic hepatitis, etc.).
  • Abnormalities of the arm or hand or radical mastectomy (preventing brachial artery ultrasound).
  • Pregnant or lactating women.

Sites / Locations

  • Stanford University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

bosentan

Pioglitazone

Arm Description

Bosentan 62.5 twice daily for 4 weeks, then 125 mg twice daily.

Pioglitazone 15 mg a day for 4 weeks then Pioglitazone 30 mg a day for the duration of the study.

Outcomes

Primary Outcome Measures

Insulin Resistance Profile Change - Triglyceride:HDL Cholesterol Ratio
insulin resistance measured -triglyceride: HDL cholesterol ratio measures at 16 weeks compared with baseline.

Secondary Outcome Measures

6 Minute Walk Test
6 minute walk test measures the distance that a patient can walk on a flat, hard surface in a period of 6 minutes.It assess the disease severity of the subject at 16 week compared to the baseline.
NYHA (New York Heart Association Classification) Changes
New York Heart Classification(NYHA) changes measured at 16 weeks compared with baseline. NYHA Classification: NYHA class I:no symptoms and no limitation in ordinary physical activity NYHA class II:Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity NYHA class III:Marked limitation in activity due to symptoms, even during less-than-ordinary activity, NYHA class IV:Severe limitations. Experiences symptoms even while at rest. {Higher NYHA class represent worse symptoms}

Full Information

First Posted
January 16, 2009
Last Updated
February 13, 2017
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT00825266
Brief Title
Insulin Resistance in Pulmonary Arterial Hypertension
Official Title
The Effect of Bosentan and Pioglitazone on Insulin Resistance in Pulmonary Arterial Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Terminated
Why Stopped
difficulty in finding eligible subjects
Study Start Date
September 2008 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate 1) the incidence of insulin resistance (a pre-diabetic state) in patients with pulmonary hypertension, and 2) test the utility of a validated PH therapy (Tracleer) versus Pioglitazone in the treatment of those patients found to have insulin resistance.
Detailed Description
The Effect of Bosentan and Pioglitazone on Insulin Resistance in Pulmonary Arterial Hypertension ,is a study evaluating the incidence of insulin resistance in patients with pulmonary hypertension and testing the utility of a validated PH therapy(Tracleer) versus Pioglitazone in the treatment of those patients found to have insulin resistance.Patients with PAH must be stable on therapy for at least 3 months are considered for enrollment in this study.With the exception of PAH, subjects must be free of major medical illnesses, including diabetes mellitus ,malignancy or significant hepatic or renal disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Pulmonary
Keywords
pulmonary hypertension & insulin resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
bosentan
Arm Type
Active Comparator
Arm Description
Bosentan 62.5 twice daily for 4 weeks, then 125 mg twice daily.
Arm Title
Pioglitazone
Arm Type
Active Comparator
Arm Description
Pioglitazone 15 mg a day for 4 weeks then Pioglitazone 30 mg a day for the duration of the study.
Intervention Type
Drug
Intervention Name(s)
bosentan
Other Intervention Name(s)
Tracleer
Intervention Description
Bosentan 62.5 mg BID for 4 weeks, then 125mg BID for duration of study.
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
Pioglitazone 15 mg a day for 4 weeks then Pioglitazone 30 mg a day for the duration fo the study.
Primary Outcome Measure Information:
Title
Insulin Resistance Profile Change - Triglyceride:HDL Cholesterol Ratio
Description
insulin resistance measured -triglyceride: HDL cholesterol ratio measures at 16 weeks compared with baseline.
Time Frame
baseline and 16 weeks
Secondary Outcome Measure Information:
Title
6 Minute Walk Test
Description
6 minute walk test measures the distance that a patient can walk on a flat, hard surface in a period of 6 minutes.It assess the disease severity of the subject at 16 week compared to the baseline.
Time Frame
Baseline and 16 weeks
Title
NYHA (New York Heart Association Classification) Changes
Description
New York Heart Classification(NYHA) changes measured at 16 weeks compared with baseline. NYHA Classification: NYHA class I:no symptoms and no limitation in ordinary physical activity NYHA class II:Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity NYHA class III:Marked limitation in activity due to symptoms, even during less-than-ordinary activity, NYHA class IV:Severe limitations. Experiences symptoms even while at rest. {Higher NYHA class represent worse symptoms}
Time Frame
Baseline and 16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with Pulmonary Arterial Hypertension (PAH) must be stable on therapy for at least 3 months prior to enrollment in the trial. We will include patients with idiopathic PAH and Familial PAH as well as PAH associated with collagen vascular disease or drug or toxin exposure. With the exception of PAH, subjects must be free of major medical illnesses, including diabetes mellitus (must have fasting plasma glucose < 126 mg/dL and taking no anti-hyperglycemic agent), malignancy or significant hepatic or renal disease. Subjects may be hypertensive and on anti-hypertensive medications as long as blood pressure is < 150/100 mm Hg. Subjects may also be dyslipidemic and/or taking drugs to improve abnormalities of lipid metabolism, but they will be excluded if they are taking medications known to alter insulin sensitivity, including glucocorticoids, niacin, anti-retrovirals, thiazolidinediones, or metformin. Use of oral contraceptives or estrogen and/or progesterone replacement therapy is permitted. Weight must be stable and the subjects agree not to change their eating habits or exercise regimen during the study period. There will be no restrictions with regard to race or socioeconomic status, and the racial/ethnic composition of the study population will be reflective of the communities surrounding the Stanford University Medical Center. Exclusion Criteria: * Vulnerable subject status. Concurrent Endothelin-1 antagonist therapy Concurrent Thiazolidinedione therapy New York Heart Class III or IV PAH related to other etiologies. Diabetes Mellitus with Fasting Glucose Levels > 126 mg/dL Allergy or hypersensitivity to pioglitazone or bosentan administration. Current treatment with statin therapy. Initiation of PAH therapy (prostacyclin analogues, phosphodiesterase-5 inhibitors) within three months of enrollment. Inability or unwillingness to avoid systemic steroid containing medications for four months. Inhaled steroid use is acceptable. Current or recent use or planned treatment with: glyburide, cyclosporine, nilotinib, nisoldipine, ranolazine, thioridazine Hepatic transaminases > 2x the upper limit of normal at the center at screening. Current or recent (< 6 months) chronic heavy alcohol consumption. Current use of another investigational drug (non-FDA approved) for PAH. Lung transplant recipients. History of myositis. Renal failure (Cr 2.0). Hospitalized or acutely ill. Chronic liver disease (cirrhosis, chronic hepatitis, etc.). Abnormalities of the arm or hand or radical mastectomy (preventing brachial artery ultrasound). Pregnant or lactating women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roham T. Zamanian
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States

12. IPD Sharing Statement

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Insulin Resistance in Pulmonary Arterial Hypertension

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