Hormonal, Metabolic, and Signaling Interactions in PAH

NCT01884051 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1899

Last updated 2025-09-16

No results posted yet for this study

Summary

Our hypothesis is that optimal treatment of the dysfunctional metabolic pathways which underlie PAH will improve pulmonary vascular function and consequences of the disease.

Conditions

  • Idiopathic Pulmonary Arterial Hypertension
  • Heritable Pulmonary Arterial Hypertension
  • Scleroderma Associated Pulmonary Arterial Hypertension
  • Appetite Suppressant Associate PAH

Sponsors & Collaborators

  • Vanderbilt University Medical Center

    lead OTHER

Principal Investigators

  • James E Loyd, MD · Vanderbilt University Medical Center

Eligibility

Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2032-07-31
Completion
2032-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01884051 on ClinicalTrials.gov