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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02966899
Other study ID # 312231
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date July 2017

Study information

Verified date December 2023
Source Providence VA Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to elucidate the relationship between myocardial right ventricular triglyceride content (steatosis) and right ventricular dysfunction in participants with pulmonary hypertension, and investigate reversibility of this phenotype with omega-3 fatty acid treatment.


Description:

The investigators propose to treat 30 participants that are identified as having elevated myocardial triglyceride content (defined as greater than 0.50%) on cardiac MRI with 4 grams of omega-3 fatty acids daily for six months with a primary end point of reducing right ventricular steatosis and a secondary endpoint of improving RV systolic function. The investigators hypothesize that right ventricular steatosis by cardiac MRI will be associated with the degree of right ventricular systolic function by cardiac MRI. In the subset of participants with elevated baseline steatosis who are treated with a lipoprotective strategy, the investigators hypothesize that six months of therapy with omega-3 fatty acids will reduce myocardial steatosis and improve right ventricular systolic function.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 30 Years and older
Eligibility Inclusion Criteria: - Adult men and women > 30 years of age with a diagnosis of pulmonary hypertension (defined as mean pulmonary arterial pressure =25 mmHg at rest on right heart catheterization) Exclusion Criteria: - Contraindication to MRI (e.g., metallic hazards or allergy to gadolinium) - Renal dysfunction (eGFR < 60 ml/min/1.73m2 as estimated by the Modified Diet in Renal Disease formula) - High risk features for nephrogenic systemic fibrosis (solitary kidney or prior renal transplant) - Active pregnancy or breastfeeding (determined by urinary pregnancy test before CMR) - Weight > 550 lb or waist diameter > 70 cm (limits for our Siemens Verio CMR system) - Fish Allergy

Study Design


Intervention

Dietary Supplement:
Omega-3 fatty acids


Locations

Country Name City State
United States Providence VA Medical Center Providence Rhode Island

Sponsors (1)

Lead Sponsor Collaborator
Wen-Chih Wu

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Right ventricular myocardial triglyceride content (by cardiac MRI) in 30 participants with pulmonary hypertension 6 months
Secondary Right ventricular ejection fraction (by cardiac MRI) in 30 participants with pulmonary hypertension 6 months
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