A Study of the Effect of Topical Testosterone Replacement Therapy on Blood Pressure in Adult Male Participants With Hypogonadism
Public ClinicalTrials.gov record NCT04274894. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
24-Hour Ambulatory Blood Pressure Monitoring Study in Hypogonadal Men Receiving Testosterone Replacement Therapy
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Hypogonadism is an endocrine disorder characterized by absent or deficient testosterone levels along with signs and symptoms of androgen deficiency, including delayed development or regression of sexual characteristics, impaired sexual function and sense of well-being, depressed mood, decreased muscle strength associated with loss of muscle mass and reduced bone mineral density. AndroGel 1.62% has demonstrated its ability to increase total testosterone levels in the blood by absorption of testosterone through the skin when applied topically. This study evaluated the effect of AndroGel 1.62% on systolic blood pressure using ambulatory blood pressure monitoring in hypogonadal men who used testosterone replacement therapy. AndroGel 1.62% is a drug used for the treatment of hypogonadism, which is associated with low or no testosterone. This was an open-label study which means that both the study doctor and study participants knew what drug and what dose is being used. All participants in this study were in the same group, called a treatment arm. Adult male participants with hypogonadism were enrolled and received AndroGel 1.62%. This was a multi-center study with 190 participants enrolled (initially planned) in approximately 45 sites in the United States to yield 171 subjects in the per protocol (PP) population. A blinded sample size re-estimation (BSSR) was performed when around 70% of the planned subjects in the PP population had completed the end of treatment visit. Sample size was increased at BSSR and 246 participants were actually enrolled. Participants received daily topical gel doses of AndroGel 1.62% for approximately 16 weeks. There may have been a higher burden for participants in this study compared to standard of care. Participants attended 8 study visits during the course of the study at a hospital or clinic and received 2 study phone calls. The effect of the treatment was checked by medical assessments, blood tests (including pharmacokinetic sampling), and 24-hour blood pressure monitors.
Study identification
- NCT ID
- NCT04274894
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 4
- Enrollment
- 246 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- Male
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- May 11, 2020
- Primary completion
- Dec 6, 2021
- Completion
- Jan 6, 2022
- Last update posted
- Dec 14, 2022
2020 – 2022
United States locations
- U.S. sites
- 45
- U.S. states
- 23
- U.S. cities
- 43
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| G & L Research, LLC /ID# 216793 | Foley | Alabama | 36535 | — |
| NewportNativeMD, Inc. /ID# 216992 | Newport Beach | California | 92663-3600 | — |
| Valley Renal Medical Group Research /ID# 216321 | Northridge | California | 91324-4622 | — |
| West Coast Research LLC /ID# 216813 | San Ramon | California | 94582 | — |
| Lynn Institute of Denver /ID# 216863 | Aurora | Colorado | 80012 | — |
| Innovative Research of West Florida /ID# 216364 | Clearwater | Florida | 33756-2004 | — |
| Seidman Clinical Trials,Delray /ID# 216794 | Delray Beach | Florida | 33484-6529 | — |
| Invesclinic, U.S., LLC /ID# 216778 | Fort Lauderdale | Florida | 33308 | — |
| Indago Research and Health Cen /ID# 216319 | Hialeah | Florida | 33012-4170 | — |
| Care Partners Clinical Research /ID# 216773 | Jacksonville | Florida | 32277 | — |
| Pharmax Research Clinic /ID# 216343 | Miami | Florida | 33126 | — |
| Care Research center Inc. /ID# 216367 | Miami | Florida | 33175 | — |
| West Orange Endocrinology /ID# 217106 | Ocoee | Florida | 34761-4547 | — |
| North Georgia Clinical Research /ID# 216864 | Woodstock | Georgia | 30189 | — |
| Solaris Clinical Research /ID# 216772 | Meridian | Idaho | 83646 | — |
| Loretto Hospital.Affnity Clinical Research Institute /ID# 216884 | Chicago | Illinois | 60644 | — |
| Affinity Clinical Research /ID# 216807 | Oak Brook | Illinois | 60523-1245 | — |
| Investigative Clinical Research of Indiana, LLC /ID# 216943 | Elwood | Indiana | 46036-3341 | — |
| Iowa Diabetes and Endocrinology Research Center /ID# 216316 | West Des Moines | Iowa | 50265 | — |
| PRN Professional Research Network of Kansas, LLC /ID# 216805 | Wichita | Kansas | 67205 | — |
| The Research Grp of Lexington /ID# 216451 | Lexington | Kentucky | 40503-2969 | — |
| Centennial Medical Group /ID# 216340 | Elkridge | Maryland | 21075 | — |
| Advanced Biomedical Research of America /ID# 216797 | Las Vegas | Nevada | 89123 | — |
| Amici Clinical Research /ID# 216779 | Warren Township | New Jersey | 07059 | — |
| NM Clinical Research & Osteoporosis Center, Inc /ID# 216808 | Albuquerque | New Mexico | 87106 | — |
| AccuMed Research Associates /ID# 216775 | Garden City | New York | 11530 | — |
| Randolph Health Internal Medicine /ID# 216366 | Asheboro | North Carolina | 27203 | — |
| OnSite Clinical Solutions, LLC /ID# 216279 | Charlotte | North Carolina | 28277 | — |
| OnSite Clinical Solutions, LLC /ID# 216368 | Charlotte | North Carolina | 28277 | — |
| Triad Clinical Trials /ID# 216792 | Greensboro | North Carolina | 27410 | — |
| Lucas Research /ID# 216487 | Morehead City | North Carolina | 28557 | — |
| Diabetes and Endocrinology Associates of Stark County Inc /ID# 216362 | Canton | Ohio | 44718 | — |
| Intend Research /ID# 216320 | Norman | Oklahoma | 73069 | — |
| Tristar Clinical Investigations PC /ID# 216944 | Philadelphia | Pennsylvania | 19114-1025 | — |
| Frontier Clinical Research /ID# 216365 | Smithfield | Pennsylvania | 15478 | — |
| New Phase Research & Development /ID# 216774 | Knoxville | Tennessee | 37909 | — |
| Clinical Neuroscience Solutions - Memphis /ID# 216790 | Memphis | Tennessee | 38119 | — |
| Arlington Family Research Center, Inc /ID# 216363 | Arlington | Texas | 76012 | — |
| Associates in Medicine, P.A. /ID# 216781 | Houston | Texas | 77027-3103 | — |
| FMC Science /ID# 216318 | Lampasas | Texas | 76550 | — |
| Discovery Clinical Trials-San Antonio /ID# 216866 | San Antonio | Texas | 78258 | — |
| Northwest Houston Clinical Research PLLC /ID# 216358 | Tomball | Texas | 77375 | — |
| Burke Internal Medicine & Research /ID# 216322 | Burke | Virginia | 22015-2234 | — |
| Manassas Clinical Research Center /ID# 216313 | Manassas | Virginia | 20110-4421 | — |
| Virginia Research Center /ID# 216341 | Midlothian | Virginia | 23114-3256 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04274894, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Dec 14, 2022 · Synced Sep 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04274894 live on ClinicalTrials.gov.