- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02958358
FDG Uptake and Lung Blood Flow in PAH Before and After Treatment With Ambrisentan
Evaluation of FDG Uptake and Pulmonary Perfusion by Positron Emission Tomography in Patients With Pulmonary Arterial Hypertension Before and After Treatment With Ambrisentan
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The overall goal of this study is to evaluate lung, large vessel, and right ventricular glucose uptake rate using 18FDG PET and distribution of pulmonary perfusion using 13NN PET in patients with pulmonary hypertension before and after treatment with ambrisentan. The investigators propose a pilot study of patients with Group I PAH. The investigators plan to complete this pilot study with 5 patients (projected enrollment of 8 to allow for drop-out rate). Taken together, the studies above demonstrate that FDG-PET can be used to detect changes associated with PAH, and to monitor response to therapy. FDG-PET is a widely available technology, and is firmly established in the field of clinical oncology. Ambrisentan is an endothelin receptor antagonist that is FDA-approved to treat patients with pulmonary arterial hypertension. Patients will be eligible for participation in this study if they have already made a decision to start treatment with ambrisentan for pulmonary hypertension. The investigators propose a physiologic study of patients who will already have made a decision to start ambrisentan therapy. Participation in the study will not alter or affect participants decisions regarding treatment.
Prior human studies evaluating response to PH-specific therapies focused only on the right ventricle. Oikawa et al. looked at the RV uptake in patients with PH and evaluated them before and after treatment with epoprostenol. Fang and colleagues used FDG-SPECT evaluate FDG uptake in the RV of patients with IPAH and PH before and after treatment with sildenafil. Both of those studies used SUV (specific uptake variable). The investigators propose to focus on the lung and the RV uptake rate (Ki) in order to provide a more robust analysis of the metabolic changes that underlie the development of pulmonary hypertension both in the right ventricle and the lung parenchyma, and to study the response to ambrisentan with FDG-PET.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Massachusetts
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Boston, Massachusetts, United States, 02114
- Massachusetts General Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Subject is male or female aged > or =18 years of age and < or =70 years.
- Subject is diagnosed with pulmonary arterial hypertension (WHO Group I, by right heart catheterization (RHC), mean PA pressure > 25 and PCWP < 15) and planning to start therapy with ambrisentan, either as de-novo monotherapy or as part of combination therapy.
- Subject has most recently undergone RHC within three months of entering the study.
- If patient has been on PAH-specific therapy, the therapy (agent and dose) has been unchanged for at least three months.
- The subject is capable of giving informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
- A signed and dated written informed consent is obtained from the subject.
- Available to complete the study.
- Able to fast for 6 hours prior to the study.
- Able to lie flat and able to perform a 30 second breath hold.
Exclusion Criteria:
- FEV1 and/or TLC < 70% predicted.
- PCWP > 15 mm Hg.
- Inability to perform the study (by primary MD or investigator assessment).
- The subject is unable to perform the respiratory maneuvers necessary for the exam.
- Subjects who have diabetes mellitus or glucose intolerance.
- Subjects who have a known contraindication to ambrisentan.
- Subjects who have a past or present disease, which as judged by the Investigators may affect the outcome of this study.
- The subject has suspected history of drugs or alcohol abuse within the six months prior to the screening visit.
- The subject is a woman of childbearing potential who is pregnant, seeking to become pregnant, or has a positive pregnancy test.
- Subject with clinical instability in the judgment of the investigator, or hospitalization for progression of pulmonary hypertension or right heart failure in the three months prior to the study.
- Subject with diagnosis of active tuberculosis, lung cancer, clinically overt bronchiectasis, allergic rhinitis, asthma, heart failure, ischemic heart disease, or COPD.
- Subject that had a respiratory tract infection in the 4 weeks prior to the screening visit and throughout the duration of the study.
- The subject has been exposed to a radiation dose over the past year that, when added to the radiation dose expected in this study, would exceed permissible yearly exposure as determined by the MGH radiation safety committee.
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Pulmonary Hypertension
Patients with Group I pulmonary arterial hypertension to undergo CT imaging, functional PET imaging before and after 3 months of treatment with ambrisentan
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Physiology study using CT and functional PET imaging with 13NN and FDG as radiotracers; images obtained before and 3 months after treatment with ambrisentan.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Coefficient of variation of perfusion
Time Frame: One imaging visit lasting up to 3 hours
|
Images will be generated with positron emission tomography that will be used to calculate the degree to which the blood flow in the lung is patchy rather than smooth.
The statistical measure of this is called the coefficient of variation.
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One imaging visit lasting up to 3 hours
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
FDG Uptake Rate (Ki)
Time Frame: One imaging visit lasting up to 3 hours
|
To determine the FDG uptake (Ki) in the right ventricle, large pulmonary vessels, and pulmonary parenchyma to investigate the effect of treatment with ambrisentan on the RV, large vessel and pulmonary parenchyma 18FDG uptake rate and its relationship to invasive hemodynamic measurements, RV function by echo, functional class, 6MWT and serum NT-proBNP levels.
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One imaging visit lasting up to 3 hours
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Robert S Harris, MD, Massachusetts General Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2013P002592
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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