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NCT01884051 · ClinicalTrials.gov registry record
Hormonal, Metabolic, and Signaling Interactions in PAH
A clinical trial of Idiopathic Pulmonary Arterial Hypertension and Heritable Pulmonary Arterial Hypertension, sponsored by Vanderbilt University Medical Center.
- Recruiting
- Registry status
- 1,899
- Enrollment target
- 1
- Study location
NCT01884051 is a study of Idiopathic Pulmonary Arterial Hypertension and Heritable Pulmonary Arterial Hypertension that is actively recruiting participants, run by Vanderbilt University Medical Center. The registered enrollment target is 1,899 participants, above the 82-participant average among 3 other Idiopathic Pulmonary Arterial Hypertension trials with a reported enrollment target (2216% higher). The trial reports 1 study location across 1 state.
The verdict
NCT01884051, a study of Idiopathic Pulmonary Arterial Hypertension and Heritable Pulmonary Arterial Hypertension, is actively recruiting participants, sponsored by Vanderbilt University Medical Center.
- RECRUITING
- Registry status
- 1,899 participants
- Enrollment target
- 1
- Study location
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 Studied
Study Locations (1)
Tennessee
- Vanderbilt University Medical Center - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,899 participants |
| Start Date | 2012-09 |
| Est. Completion | 2032-07 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01884051
The ClinicalTrials.gov registry entry for NCT01884051 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 1,899 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 82-participant average among 3 other Idiopathic Pulmonary Arterial Hypertension trials with a reported enrollment target (2216% higher). The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Idiopathic Pulmonary Arterial Hypertension appearing as the primary indexed condition, and to 0 interventions.
NCT01884051 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT01884051 about?
NCT01884051 is a clinical study titled "Hormonal, Metabolic, and Signaling Interactions in PAH". Our hypothesis is that optimal treatment of the dysfunctional metabolic pathways which underlie PAH will improve pulmonary vascular function and consequences of the disease.
What is the current status of trial NCT01884051?
This trial is currently recruiting. The enrollment target is 1,899 participants. The study started on 2012-09. Estimated completion is 2032-07.
What conditions does trial NCT01884051 study?
This clinical trial studies the following conditions: Idiopathic Pulmonary Arterial Hypertension, Heritable Pulmonary Arterial Hypertension, Scleroderma Associated Pulmonary Arterial Hypertension, Appetite Suppressant Associate PAH.
Who is sponsoring clinical trial NCT01884051?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01884051 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.