๐๏ธ Verified NIH Record โข Updated 2026-03-25
Effect of Prolonged (72 Hour) Glucagon Administration on Energy Expenditure in Healthy Obese Subjects (NCT03139305)
๐ต Active, Not Recruiting Phase1 ๐ Investigational Drug / Biologic Sponsor: AdventHealth Translational Research Institute
๐ฉบ Plain-English Summary (8th-Grade Level)
The main purpose of this study is to examine the effect of prolonged (72 hour) administration of glucagon compared to placebo on energy expenditure in healthy, non-diabetic, obese subjects.
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (11 items) and avoid the listed exclusions (25 items).
Location: Translational Research Institute for Metabolism and Diabetes โ Orlando, Florida
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria
- Treatment with any medication known to significantly impact body weight or energy metabolism (e.g., weight loss medications, atypical antipsychotics) within 3 months prior to screening except for stable physiological hormone replacement therapy (i.e., thyroid hormone, estrogen).
- Treatment with a selective serotonin reuptake inhibitor, a medication for depression or apomorphine within one week prior to screening due to interaction with Zofran.
- History of bariatric surgery.
- Current liver, renal, pulmonary, cardiac, oncologic, metabolic, gastrointestinal, or hematologic disease which the Investigator believes is clinically significant, including: a. Liver disease or liver injury as indicated by abnormal liver function tests (aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, serum bilirubin) \>3 ร upper limit of normal (ULN), or history of hepatic cirrhosis.
- Impaired renal function as indicated by an estimated glomerular filtration rate (eGFR) \<60 mL/min or urine albumin-to-creatinine ratio \>35 mg/mmol.
- Significant cardiovascular disease, including Class III or greater congestive heart failure (CHF), coronary artery disease, second degree or greater heart block, or clinically significant arrhythmias; baseline second degree or greater heart block or prolonged QT syndrome (QTc interval โฅ470 msec); or any major cardiovascular event within the last 3 years (including myocardial infarction \[MI\], transient ischemic attack, cerebrovascular accident \[CVA\], angina, and hospitalization due to CHF,transient ischemic attack, and CVA).
- Metabolic, or other endocrine disorders, including diagnosis of type 1 or type 2 diabetes mellitus \[HbA1c โฅ6.5%\]), inadequately treated hyperthyroidism (thyroid stimulating hormone \[TSH\] below normal range) or hypothyroidism (TSH \>ULN \<10 U/mL and symptomatic or TSH \>10 U/mL), Cushing's disease/syndrome, Addison's disease, hypogonadism, or genetic disorders linked to obesity.
- History of irritable bowel disease, recurrent nausea, or vomiting.
- Anemia (hemoglobin \<12 g/dL in males, \<11 g/dL in females).
- History of dyslipidemia: Fasting triglycerides (TG) \>500 mg/dL and low-density lipoproteins (LDL) \>250 mg/dL.
- Self-reported history of infection with hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV).
๐ Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
๐ All Participating Trial Locations (1 Sites)
- Translational Research Institute for Metabolism and Diabetes โ Orlando, Florida
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.