Phase 2
N=5
Ghrelin Repeated Dose Study
Frailty in Aging
Bottom Line
View on ClinicalTrials.gov: NCT01833078 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Oct 2015
Primary outcome: Primary: Safety — 4 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- ghrelin (Drug)
- Age
- Older Adult · 70+ yrs
- Sex
- All
- Sponsor
- University of Pennsylvania
- Primary completion
- Jun 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Safety |
4 | — |
| SECONDARY Sustainability of Increased Caloric Intake |
691; 839 | — |
Summary
Frailty is a geriatric syndrome leading to physical deterioration including muscle wasting (sarcopenia) and unintentional weight loss. There are currently no approved therapies for frailty. Ghrelin is a hormone produced by the stomach that stimulates appetite centers in the brain. The investigators already know that a single dose of Ghrelin improves food intake immediately after the dose in frail older people. In this study, the investigators are trying to find out if repeated daily doses of ghrelin will help frail older people improve food intake for multiple days in a row.
Eligibility Criteria
Inclusion Criteria
- Individuals with three, four or five frailty criteria using the Fried frailty criteria
Exclusion Criteria
- Diabetes mellitus or fasting glucose ≥ 126 mg/dL
- Hospitalization for stroke, myocardial infarction, coronary artery bypass graft surgery, vascular surgery in the past six months.
- New York Heart Association Class III or IV congestive heart failure
- Therapy for cancer in the past 12 months, except non-melanoma skin cancer
- BMI ≥ 30 kg/m2
- Current use of corticosteroids other than topical, ophthalmic, and inhaled preparations
- Therapy with megestrol acetate or dronabinol within the last 6 weeks
- Thyroid stimulating hormone measured as 2x upper limit of normal)
- Hemoglobin 11 on the Geriatric Depression Questionnaire)
Data sourced from ClinicalTrials.gov (NCT01833078). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.