GLIDE-HF
Not yet recruitingGLP-1/GIP Receptor Agonists in Obesity-Related HFpEF: The GLIDE-HF Registry
GLIDE-HF Registry: A Prospective, Single-Center, Observational Cohort of Patients With Obesity-Related Heart Failure With Preserved Ejection Fraction, With GLP-1/GIP Receptor Agonist Therapy as an Observed Exposure and Serial Exercise Echocardiographic Phenotyping
Lead sponsor
Assets
Dulaglutide / Liraglutide / Semaglutide / Tirzepatide
Listed sites
1
Recruiting sites
-
Estimated enrollment
150
Study population
Heart failure, Hypertension, Obesity / overweight
Eligibility highlights
•Established HF
Primary endpoint
•Trajectory of exercise E/e' over time in GLP-1/GIP-exposed patients
Registered trial locations
Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Who this study enrolls
Who can enroll
Study population text
Unselected patients with obesity-related HFpEF managed in a heart failure and cardiology outpatient clinic, enrolled regardless of whether they receive GLP-1/GIP receptor agonist therapy. Obesity-related HFpEF is defined by chronic heart failure symptoms or exertional dyspnea, BMI at least 30 kg/m2, LVEF at least 50%, and objective evidence of HFpEF (no low-probability result on either the H2FPEF or HFA-PEFF score), without a dominant alternative cause of dyspnea.
Inclusion criteria
Age 18 years or older Body mass index (BMI) 30 kg/m2 or greater Symptomatic exertional dyspnea, fatigue, or reduced exercise tolerance Left ventricular ejection fraction 50% or greater Probable or established HFpEF per the diagnostic score algorithm (no low-probability result on either the H2FPEF or HFA-PEFF score) Able to perform semi-supine bicycle exercise echocardiography Written informed consent for registry participation and data processing
Exclusion criteria
Significant valvular heart disease Cardiomyopathy other than the typical HFpEF phenotype (suspected amyloidosis, restrictive or hypertrophic cardiomyopathy as the primary problem) Recent acute decompensated heart failure or recent hospitalization for heart failure Unstable coronary artery disease Severe pulmonary disease as the primary cause of dyspnea Severe anemia or another systemic cause of exercise limitation Inability to safely perform an exercise test Very poor echocardiographic window precluding any analysis Active malignancy or gynecological condition that may substantially affect CA-125 (diagnosed endometriosis, pelvic inflammatory disease, suspected ovarian tumor, significant non-cardiac ascites) Absence of consent for registry participation and data processing
Endpoints (14)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Heart failure
3 endpointsTrajectory of KCCQ Clinical Summary Score
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of NT-proBNP
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of 6-minute walk distance
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Safety / tolerability / PK
1 endpointSafety and tolerability of GLP-1/GIP receptor agonist therapy
Time frame:Baseline through 52 weeks
descriptive
Other clinical outcomes
1 endpointFeasibility of serial exercise echocardiography and lung ultrasound
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Other (unclassified)
9 endpointsTrajectory of exercise E/e' over time in GLP-1/GIP-exposed patients
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of peak tricuspid regurgitation velocity
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of LVOT VTI reserve
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of post-exercise lung ultrasound B-line count
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of transferrin saturation
Time frame:Baseline, 12, 24, and 52 weeks
ratio, improvement
Trajectory of serum ferritin
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Prevalence of iron deficiency
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Trajectory of TAPSE/PASP ratio
Time frame:Baseline, 12, 24, and 52 weeks
ratio, improvement
Trajectory of right ventricular free-wall longitudinal strain
Time frame:Baseline, 12, 24, and 52 weeks
descriptive
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the November 5, 2026 snapshot.