Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 1:19 PM
Ignite Modification Date:
2025-12-26 @ 1:19 PM
NCT ID:
NCT00675506
Eligibility Criteria:
Inclusion Criteria:
* Body mass index (BMI) greater than or equal to 30 kg/m2
* Waist circumference greater than or equal to 102 cm in men and greater than or equal to 88 cm in women
* Relative growth hormone (GH) deficiency, defined as a peak GH value of less than or equal to 8 ng/mL on Arginine-GHRH stimulation test
* Hemoglobin level greater than 12.0 g/dL
* Serum glutamic oxaloacetic transaminase and serum glutamic pyruvic transaminase less than 2.5 times the upper limit of normal
* Creatinine level less than 1.5 mg/dL
* Follicle stimulating hormone less than 20 IU/L in women
* Negative mammogram within 1 year of study entry for women older than 40 years of age
Exclusion Criteria:
* Obesity due to a known secondary cause (e.g., Cushing's syndrome, hypothyroidism) or a history of gastric bypass procedure
* Known hypersensitivity to GHRH 1-44 (TH9507)
* Known history of diabetes, fasting blood sugar less than 125 mg/dL, or antidiabetic drug use
* Using any weight lowering drugs
* Using estrogen, hormone replacement therapy, oral contraceptives, testosterone, glucocorticoids, anabolic steroids, GHRH, GH, or insulin-like growth factor-1 (IGF-1) within 3 months of study entry
* Changes in lipid lowering or antihypertensive regimen within 3 months of study entry
* Long-term illness, including anemia, chronic kidney disease, and liver disease
* History of cancer (except patients with surgically cured basal cell or squamous cell skin cancers) or history of abnormalities on age appropriate malignancy screen, including mammography, colonoscopy, and prostate exam (or prostate specific antigen greater than 5 ng/mL)
* History of hypopituitarism, pituitary surgery, pituitary/brain radiation, traumatic brain injury, or any other condition known to affect the growth hormone axis
* History of any recent cardiovascular event, including heart attack, stroke, transient ischemic attack, unstable angina pectoris, or oxygen-dependent severe pulmonary disease, within 3 months of study entry
* Clinical depression or other psychiatric illness that will not allow completion of the study as per investigator's judgement
* History of or current eating disorder
* History of recent alcohol or substance abuse (less than 1 year before study entry)
* Positive pregnancy test or breastfeeding females and positive fecal occult blood test
* Women of childbearing potential not currently using nonhormonal birth control methods, including barrier methods (e.g., IUD, condoms, diaphragms) or abstinence
* Currently enrolled in another investigational device or drug trial(s) or has received other investigational agent(s) within 28 days of study entry
* Any condition that would make this clinical trial detrimental to the patient, as judged by the patient's physician
* History of noncompliance with other therapies
* Any condition in which compliance with the study protocol is unlikely
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
55 Years
Study:
NCT00675506
Study Brief:
Protocol Section:
NCT00675506