Growth Hormone Secretagogue MK-0677 Effect on IGF-1 Levels in ESRD Patients

Completed · Not applicable · Has a placebo group

Conditions studied: Chronic Kidney Disease, End Stage Renal Disease

In brief

The objective of this study is to determine MK-0677 increases IGF-1 in patients with end stage renal disease (ESRD) on hemodialysis.

Key facts

Study ID

NCT00395291

Run by

University of Virginia

People needed

49

Starts

2006-08-01

Expected to finish

2010-05-01

Last updated by the study team

2017-02-20

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• GFR by the MDRD estimate < 30ml/minute/1.73m2 or on hemodialysis

You may not qualify if…

• Body mass index greater than 35 kg/m2, or morbid obesity
• Uncontrolled hypothyroidism, defined as an elevated serum thyroid stimulating hormone (THS) and a free serum thyroxine (T4) less than the lower limit of normal, when tested at baseline (Patients requiring thyroid replacement during the study may continue.)
• Uncontrolled hyperthyroidism, defined as a TSH less than the lower limit of normal and an elevated free T4, when tested at baseline
• Hemoglobin <10 Gm/dl
• Elevated serum transaminases (>2.0 times the upper limit of normal at baseline)
• Diabetes with one of more of the following:
• Poorly controlled diabetes as defined by a HbA1C > 7.0% at baseline)
• Proliferative diabetic retinopathy [To participate in this study, diabetic patients will need to have had a dilated ophthalmology exam within 12 months of enrollment. Individuals who already have extensive background retinopathy will need to have a dilated ophthalmology exam within the 3 months of enrollment. Patients with pre-proliferative or proliferative retinopathy will be excluded].
• Unwilling or unable to check blood glucose at home at least daily.
• Currently receiving a systemic corticosteroid dose of >10 mg prednisone (or equivalent), or patient has received, for a duration > 30 days in the previous 6 months (i.e., prior to signing the informed consent form), a systemic corticosteroid dose of > 10 mg prednisone (or equivalent). (The previous use, or current use, of a topical or inhaled corticosteroid is allowed.)
• Currently taking or previously on an anabolic steroid or growth hormone at any dose, or for any duration, during the 12 months prior to study entry.
• Significant end-organ disease, other than kidney disease, which, in the opinion of the investigator may pose an added risk to the patient, confound the study results, or impair the patient's ability to complete the trial.
• Any of the following disorders within 6 months prior to baseline:
• Acute coronary syndrome (e.g., myocardial infarction or unstable angina)
• Coronary artery intervention (e.g., coronary bypass graft [CABG], percutaneous transluminal coronary angioplasty [PTCA]).
• Stroke or transient ischemic neurological disorder (e.g. transient ischemic attack [TIA])
• New or worsening signs or symptoms of coronary heart disease within the 3 months prior to baseline.
• NYHA (New York Heart Association)Class III or IV congestive heart failure (definitions shown in Appendix A)
• Uncontrolled hypertension when checked at screening visit: as evidenced by > 160 systolic and/or 100 diastolic (measured in dominant or non-dialysis access arm, after at least 5 minutes, sitting)
• Cancer, or diagnosis of malignancy within the last 5 years, except for adequately treated basal cell or squamous cell skin cancer, or adequately treated in situ cervical cancer.
• Active carpal tunnel syndrome
• Patient is, in the opinion of the investigator, mentally or legally incapacitated such that informed consent cannot be obtained or such that adherence to the study procedures and dosing regimens is questionable.
• Patient is, at study entry, a regular user (including "recreational use") of illicit drugs or had a recent history (within the last 5 years) of drug or alcohol abuse.
• Patient plans to relocate or change to a different dialysis center during the study, rendering follow-up per protocol, impractical.
• Patient is participating in, or has participated in, another study with an investigational drug within 30 days prior to signing the informed consent form.

Where it is running

• University of Virginia — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.