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GLIDE-HF

Not yet recruiting

GLP-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

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

NCT IDNCT07787936
Org study IDGLIDE-HF-MCZ-2026-01
Secondary IDEthicsKomisja Bioetyczna przy Dolnoslaskiej Izbie Lekarskiej

Timeline

Milestones

Study first posted2026-08-26actual
Last update posted2026-08-26actual
Study start2027-01-01estimated
Primary completion2031-01-01estimated
Study completion2033-01-01estimated

Assets

Investigational agents

Who this study enrolls

Heart failureHypertensionObesity / overweight

Who can enroll

Minimum age18 Years
SexAll
Healthy volunteersNot accepted
Sampling methodNon probability sample

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

Other (unclassified)
9
Heart failure
3
Safety / tolerability / PK
1
Other clinical outcomes
1

Heart failure

3 endpoints
Secondary/protocol endpoint

Trajectory of KCCQ Clinical Summary Score

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint

Trajectory of NT-proBNP

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint

Trajectory of 6-minute walk distance

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Safety / tolerability / PK

1 endpoint
Secondary/protocol endpoint

Safety and tolerability of GLP-1/GIP receptor agonist therapy

Time frame:Baseline through 52 weeks

descriptive

Other clinical outcomes

1 endpoint
Other/protocol endpoint

Feasibility of serial exercise echocardiography and lung ultrasound

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Other (unclassified)

9 endpoints
Primary/protocol endpoint/low confidence

Trajectory of exercise E/e' over time in GLP-1/GIP-exposed patients

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Trajectory of peak tricuspid regurgitation velocity

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Trajectory of LVOT VTI reserve

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Trajectory of post-exercise lung ultrasound B-line count

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Trajectory of transferrin saturation

Time frame:Baseline, 12, 24, and 52 weeks

ratio, improvement

Secondary/protocol endpoint/low confidence

Trajectory of serum ferritin

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Prevalence of iron deficiency

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Secondary/protocol endpoint/low confidence

Trajectory of TAPSE/PASP ratio

Time frame:Baseline, 12, 24, and 52 weeks

ratio, improvement

Secondary/protocol endpoint/low confidence

Trajectory of right ventricular free-wall longitudinal strain

Time frame:Baseline, 12, 24, and 52 weeks

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateNovember 5, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.