RECRUITING

PET Image in PAH Patients

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Pulmonary arterial hypertension (PAH) is mortal disease affecting the blood vessels of the lung. Despite its morbid prognosis, PAH is often misdiagnosed or ignored, with an average time of 44 months between onset of symptoms to diagnosis and substantial progression of disease severity. Therefore, a pressing need exists to develop non-invasive diagnostic imaging tools, particularly that can detect early disease stages. Efforts have been made to develop such imaging capabilities through platform development of echocardiography, cardiac MRI, chest computed tomography (CT), and positron emission tomography (PET), among others. While some have demonstrated promise, few have shown a precise ability to offer disease quantifications of the diseased lung and vasculature itself, to detect early stages of disease, and to reflect alterations of the lung, vasculature, and right ventricle that reflect the molecular origins of this disease. \[F-18\]FGln has been previously utilized in oncology studies as a non-invasive in vivo imaging biomarker of tumor glutamine flux and metabolism. Our preliminary in vivo pre-clinical rodent studies demonstrated that \[F-18\]FGln demonstrated increased uptake in diseased pulmonary vessels and the right ventricle in a rodent model of PAH. The proposed research study will provide preliminary evidence of the potential to utilize \[F-18\]FGln as a non-invasive imaging biomarker of glutamine flux and metabolism across a range of PAH subjects.

Official Title

Utilizing 18F-fluoroglutamine PET Imaging in Patients With Pulmonary Arterial Hypertension

Quick Facts

Study Start:2022-07-11
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05452889

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age between 18-75 years old
  2. 2. Confirmed diagnosis of SSc-PAH / SSc-eiPAH/IPAH/ by right heart catheterization. And Scleroderma with no PAH confirmand by echo.
  3. 1. Age between 18-75 years old
  4. 2. Individuals who are at low risk for current or future cardiovascular or pulmonary symptoms or diseases
  1. 1. Smoking
  2. 2. Pregnant/ breast feeding women
  3. 3. Children under 18
  4. 4. Inability to read and understand the informed consent
  5. 5. History of CT contrast allergy
  6. 6. Inability to lie down for long period of time
  7. 7. Having claustrophobic
  8. 8. History of radiation exposure at workplace
  9. 9. Consuming more than 2-3 alcoholic drinks a week
  10. 10. Working previously in any of the following "cool miner, painter, iron miner, Mill worker, asbestos, insulation/heat resistance materials, sand"
  11. 11. Any medical conditions involving the heart or lungs that would make participation in the study unsafe in the opinion of the PI.
  12. 1. Smoking
  13. 2. Pregnant/ breast feeding women
  14. 3. Children under 18
  15. 4. Inability to read and understand the informed consent
  16. 5. History of CT contrast allergy.
  17. 6. Inability to lie down for long period of time
  18. 7. Having claustrophobic
  19. 8. History of radiation exposure at workplace
  20. 9. Consuming more than 2-3 alcoholic drinks a week
  21. 10. Working previously in any of the following "coal miner, painter, iron miner, Mill worker, asbestos, insulation/heat resistance materials, sand"
  22. 11. Any medical conditions involving the heart or lungs or that would make participation in the study unsafe in the opinion of the PI.
  23. 12. Family history of Pulmonary Hypertension or Scleroderma

Contacts and Locations

Study Contact

Yassmin Al Aaraj
CONTACT
14126479227
yaa29@pitt.edu
Stephen Chan
CONTACT
chansy@upmc.edu

Principal Investigator

Stephen Chan
PRINCIPAL_INVESTIGATOR
University of Pittsburgh

Study Locations (Sites)

Montefiore Hospital Clinical and Translational Research Center
Pittsburgh, Pennsylvania, 15213
United States

Collaborators and Investigators

Sponsor: Stephen Y. Chan

  • Stephen Chan, PRINCIPAL_INVESTIGATOR, University of Pittsburgh

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-07-11
Study Completion Date2025-12

Study Record Updates

Study Start Date2022-07-11
Study Completion Date2025-12

Terms related to this study

Keywords Provided by Researchers

  • Pulmonary hypertension
  • Early diagnoses
  • Non invasive

Additional Relevant MeSH Terms

  • Pulmonary Arterial Hypertension