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Hormone Therapy
androgel for Hypogonadotrophic Hypogonadism
N/A
Waitlist Available
Led By Paresh Dandona
Research Sponsored by University at Buffalo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
Study Summary
The purpose of this study is to examine the effects of testosterone deficiency in men with diabetes on atherogenesis, inflammation, cardiovascular Risk factors And adiposity .
Eligible Conditions
- Hypogonadotrophic Hypogonadism
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Carotid Intima Media Thickness
Secondary outcome measures
Endothelial Function
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: androgelExperimental Treatment1 Intervention
androgel
Group II: no treatmentActive Control1 Intervention
eugonadal comparison arm
Group III: placeboPlacebo Group1 Intervention
placebo gel
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Testosterone
FDA approved
Find a Location
Who is running the clinical trial?
Solvay PharmaceuticalsIndustry Sponsor
131 Previous Clinical Trials
37,307 Total Patients Enrolled
University at BuffaloLead Sponsor
132 Previous Clinical Trials
98,932 Total Patients Enrolled
Paresh DandonaPrincipal InvestigatorKaleida Health
1 Previous Clinical Trials
30 Total Patients Enrolled
Frequently Asked Questions
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