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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03826160
Other study ID # 2018P001792
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 30, 2019
Est. completion date April 19, 2022

Study information

Verified date July 2022
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardiac steatosis is increased among individuals with HIV, and may predispose to cardiac mechanical dysfunction and subsequent heart failure. The pathogenesis and treatment of cardiac steatosis is not well understood. The investigators have previously shown that perturbed growth hormone (GH) secretion in HIV contributes to ectopic fat accumulation in the viscera and the liver. Moreover, the investigators have found that augmentation of endogenous GH secretion with the FDA-approved medication tesamorelin reduces visceral and hepatic fat. In this longitudinal observational study, the investigators will examine patients with HIV and abdominal fat accumulation who either plan or do not plan to initiate tesamorelin prescribed clinically. The investigators hypothesize that blunted GH secretion in HIV is associated with cardiac steatosis. The investigators also hypothesize that use of tesamorelin for 6 months is associated with a reduction in intramyocardial fat and preserved cardiac function.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date April 19, 2022
Est. primary completion date April 19, 2022
Accepts healthy volunteers
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - Men and women, ages 40-70 years - Documented HIV infection on stable antiretroviral therapy for = 3 months - Abdominal obesity with waist circumference = 102 cm in men, = 88 cm in women - Indication for tesamorelin per clinical judgment Exclusion Criteria: - CD4 < 100 cells/mm3 or HIV viral load > 400 copies/mL - Current active AIDS-defining illness - History or symptoms consistent with heart failure - Standard contraindications to MRI including severe allergy to gadolinium - Glomerular filtration rate (eGFR) < 45 mL/min/1.73 m2 within one month of MRI study - Use of growth hormone-releasing hormone (GHRH) or growth hormone (GH) within the past 6 months - HbA1c > 7%, chronic insulin use within the past 6 months, and/or change in anti-diabetic agents within the past 3 months - Change in statin therapy within the past 3 months - Chronic corticosteroid use except intermittent topic steroid creams or inhalers - Pregnancy or breastfeeding

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intramyocardial lipid content Measure of fat content within cardiac muscle as assessed by cardiac magnetic resonance spectroscopy (MRS) 6 months
Secondary Circumferential diastolic strain rate Measure of diastolic function as assessed by cardiac magnetic resonance imaging (MRI) 6 months
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