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:
2025-12-25 @ 3:20 AM
Ignite Modification Date:
2025-12-25 @ 3:20 AM
NCT ID:
NCT02748005
Eligibility Criteria:
Inclusion Criteria:
1. Agrees to written as well as audio-visual informed consent.
2. Ability to understand the risks/benefits of the protocol
3. Male between 35-65 years of age.
4. Diagnosed with Symptomatic hypogonadism
Exclusion Criteria:
1. Uncooperative Subjects
2. Impaired hepatic function indicated by SGOT/SGPT \>2.5 times the upper limit of normal.
3. Abnormal liver or kidney function tests (ALT or AST \> 2 times the upper limit of normal
4. elevated creatinine, males \> 125 µmol/L or 1.4mg/dl, females \> 110 µmol/L or1.2mg/dl)
5. Patients suffering from CAD
6. History of malignancy
7. History of hypersensitivity to any of the investigational drugs Receiving any other testosterone booster therapy/medication/supplement within the last 2 months
8. History of coagulopathies
9. High alcohol intake (\>2 standard drinks per day)
10. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
11. Any medical condition, where the investigator feels participation in the study could be detrimental to the subjects overall well-being
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
35 Years
Maximum Age:
65 Years
Study:
NCT02748005
Study Brief:
Protocol Section:
NCT02748005