The Expression and Significance of MiRNA

Sponsor
Megan Ballinger (Other)
Overall Status
Completed
CT.gov ID
NCT00806312
Collaborator
(none)
207
1
121.5
1.7

Study Details

Study Description

Brief Summary

It is not always known what causes PAH or what the best treatment is. The doctors doing this study would like to understand more about why some people develop PAH and other do not. They also would like to learn more about which treatments might help PAH and which people might respond better to treatments.

Doctors think that testing certain substances found in blood cells might help answer these questions. These substances are normally released by our bodies to protect us from infection and to tell the difference between normal and foreign substances in our body. Finally, a new test will study very small molecules called microRNA that control how our genes are expressed. This study is being done to see if blood samples can be tested to determine who might develop PAH, how well drugs will work to treat PAH and to learn more about the development of PAH.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    You will be asked to donate blood when you have your right heart catheterization and also at the 3-4 month follow-up visit. The amount of blood collected during your heart catheterization is about 20cc (about 4 teaspoons). This blood is discarded as part of the clinical catheterization procedure, but we are asking that we use it for this research study. Then, at the follow-up right heart catheterization, you will be asked to donate 20 cc (which is about 4 teaspoons) of blood.

    If the second right heart is not required for clinical purposes then you will be asked to give a blood sample during your 3-4 month follow up clinic visit.

    If you require an additional right heart catheterization, within one year, we will ask that you donate additional samples at the subsequent RHC.

    Other data collected as part of your clinical care, such as medical history, chest x-ray (picture of your lungs), echocardiogram (picture of your heart), ventilation perfusion scan (determines how much blood goes to your lungs), chest CT (thin pictures of my lungs as slices), pulmonary function tests (breathing tests), and lab blood tests, will be used as part of this research.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    207 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Expression and Significance of miRNA Profile and Markers of Inflammation in Patients With Pulmonary Arterial Hypertension
    Study Start Date :
    Jul 1, 2008
    Actual Primary Completion Date :
    Aug 16, 2018
    Actual Study Completion Date :
    Aug 16, 2018

    Arms and Interventions

    Arm Intervention/Treatment
    1 PAH

    Patients who are ≥ 18 years of age, not pregnant, and undergoing right heart catheterization for PAH diagnosis as part of their clinical care will be approached for consent and participation in this study.

    2. Control

    Patients who present with symptoms of PAH and whose clinical right heart catheterization doesn't support this diagnosis will be enrolled as control subjects.

    Outcome Measures

    Primary Outcome Measures

    1. evaluate if miRNa profile and markers of inflammation in patients with PAH. These profiles may enable us differentiate patients that have PAH. This may assist in predicting response to therapy and enable us to optimize their treatment. may also shed s [end of study]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • ≥ 18 years of age

    • Not pregnant

    • Undergoing right heart catheterization for PAH diagnosis

    Exclusion Criteria:
    • Pregnant

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Ohio State University Columbus Ohio United States 43210

    Sponsors and Collaborators

    • Megan Ballinger

    Investigators

    • Principal Investigator: Namita Sood, MD, Ohio State University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Megan Ballinger, Research Assistant Professor, Ohio State University
    ClinicalTrials.gov Identifier:
    NCT00806312
    Other Study ID Numbers:
    • 2008H0070
    First Posted:
    Dec 10, 2008
    Last Update Posted:
    Nov 2, 2021
    Last Verified:
    Oct 1, 2021
    Keywords provided by Megan Ballinger, Research Assistant Professor, Ohio State University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 2, 2021