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We did not accrue as much as anticipated and the PI (Dabaja) is no longer at Weill Cornell.
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This is a randomized controlled trial to evaluate the effect of ramipril in stimulating and promoting sperm production in men with low sperm count. Ramipril is an Angiotensin Converting Enzyme Inhibitor (ACEI) currently used to treat high blood pressure. However, previous studies have shown that this class of medications can improve sperm parameters. The purpose of this study is to evaluate the efficacy of ramipril compared to placebo (Substance That is not known to have treatment effect), in improving sperm density in infertile men with documented low sperm count. This study will help us identify subjects that might benefit from treatment with this medication, and the effect it will have on sperm count, shape, and motility.
Approximately half of all infertility problems are caused by male factors. These men account for 17% of patients at the primary health care level that seek help for infertility. Oligospermia (Low sperm count) of unknown cause occurs in up to 60% of men with unexplained infertility. Certain group of patients with oligospermia can father children, but those with infertility have long posed a major therapeutic challenge. A variety of empirical non-specific treatments have been used, in attempt to improve their semen characteristics and fertility. In the past, androgens were suggested as a treatment; however, exogenous testosterone was found to exert negative feedback on the pituitary-gonadal axis and thereby suppresses Follicle Stimulating Hormone (FSH) and Luteinizing Hormone (LH) secretion then adversely affects sperm production. Other treatment modalities like clomiphene citrate, tamoxifen, recombinant FSH, zinc, selenium, and L-carnitine have been tried with minimal success. In the present study we are proposing the use of an angiotensin converting enzyme inhibitor (ACEI) for the treatment of oligospermia. A recently published pilot study showed that the use of lisinopril improved sperm quantity and quality in oligospermic men. ACEI are inexpensive, safe, widely available, and, if effective in improving sperm production and quality, could avert couples from undergoing invasive procedures.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ramipril | Experimental | The initial dose of ramipril will be 2.5 mg that will be started at visit 2, week zero of the study. The dose will be increased to 5 mg during visit 3, 4 weeks into the study, for a total of 32 weeks. |
|
| Placebo | Sham Comparator | The placebo group will get a similar pill that will be started at visit 2, week zero of the study. Subjects will be asked to double the dose by taking two pills during visit 3, four weeks into the study, for a total of 32 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ramipril | Drug | Angiotensin Converting Enzyme Inhibitor |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Sperm Density in Infertile Men With Documented Oligospermia. | 32 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Total Motile Sperm Count(TMSC), Total Sperm Count, Sperm Motility, and Morphology in the Ejaculate. | The efficacy of ramipril in improving total sperm count will be evaluated, as well as, improving sperm motility, and morphology. | 32 weeks |
| Pregnancy Rate |
| Measure | Description | Time Frame |
|---|---|---|
| Seminal Angiotensin II and Serum Bradykinin Levels | 32 weeks |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Peter N Schlegel, MD | Weill Medical College of Cornell University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Weill Cornell Medical College, Department of Urology | New York | New York | 10065 | United States |
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| Label | URL |
|---|---|
| Department of Urology Cornell | View source |
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| ID | Title | Description |
|---|---|---|
| FG000 | Ramipril | The initial dose of ramipril will be 2.5 mg that will be started at visit 2, week zero of the study. The dose will be increased to 5 mg during visit 3, 4 weeks into the study, for a total of 32 weeks. Ramipril: Angiotensin Converting Enzyme Inhibitor |
| FG001 | Placebo | The placebo group will get a similar pill that will be started at visit 2, week zero of the study. Subjects will be asked to double the dose by taking two pills during visit 3, four weeks into the study, for a total of 32 weeks. Placebo: Placebo pill that will match the treatment pill |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Ramipril | The initial dose of ramipril will be 2.5 mg that will be started at visit 2, week zero of the study. The dose will be increased to 5 mg during visit 3, 4 weeks into the study, for a total of 32 weeks. Ramipril: Angiotensin Converting Enzyme Inhibitor |
| BG001 | Placebo |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Sperm Density in Infertile Men With Documented Oligospermia. | Data was not collected on the 2 participants as the principal investigator on this trial moved to a different practice and thus the study terminated before any results could be analyzed. | Posted | 32 weeks |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Ramipril | The initial dose of ramipril will be 2.5 mg that will be started at visit 2, week zero of the study. The dose will be increased to 5 mg during visit 3, 4 weeks into the study, for a total of 32 weeks. Ramipril: Angiotensin Converting Enzyme Inhibitor |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Peter N Schlegel, MD | Weill Cornell Medical College | 2127465491 | pnschleg@med.cornell.edu |
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| ID | Term |
|---|---|
| D009845 | Oligospermia |
| D000072660 | Teratozoospermia |
| D053627 | Asthenozoospermia |
| D007248 | Infertility, Male |
| ID | Term |
|---|---|
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007246 | Infertility |
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| ID | Term |
|---|---|
| D017257 | Ramipril |
| D000073893 | Sugars |
| ID | Term |
|---|---|
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D002241 | Carbohydrates |
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| Placebo | Drug | Placebo pill that will match the treatment pill |
|
|
| 32 weeks |
| Hormonal Profile | LH, FSH, serum testosterone, prolactin | 32 weeks |
The placebo group will get a similar pill that will be started at visit 2, week zero of the study. Subjects will be asked to double the dose by taking two pills during visit 3, four weeks into the study, for a total of 32 weeks. Placebo: Placebo pill that will match the treatment pill |
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
|
| Secondary | Total Motile Sperm Count(TMSC), Total Sperm Count, Sperm Motility, and Morphology in the Ejaculate. | The efficacy of ramipril in improving total sperm count will be evaluated, as well as, improving sperm motility, and morphology. | Data was not collected on the 2 participants as the principal investigator on this trial moved to a different practice and thus the study terminated before any results could be analyzed. | Posted | 32 weeks |
|
|
| Secondary | Pregnancy Rate | Data was not collected on the 2 participants as the principal investigator on this trial moved to a different practice and thus the study terminated before any results could be analyzed. | Posted | 32 weeks |
|
|
| Secondary | Hormonal Profile | LH, FSH, serum testosterone, prolactin | Data was not collected on the 2 participants as the principal investigator on this trial moved to a different practice and thus the study terminated before any results could be analyzed. | Posted | 32 weeks |
|
|
| Other Pre-specified | Seminal Angiotensin II and Serum Bradykinin Levels | Data was not collected on the 2 participants as the principal investigator on this trial moved to a different practice and thus the study terminated before any results could be analyzed. | Posted | 32 weeks |
|
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| 0 |
| 1 |
| 0 |
| 1 |
| EG001 | Placebo | The placebo group will get a similar pill that will be started at visit 2, week zero of the study. Subjects will be asked to double the dose by taking two pills during visit 3, four weeks into the study, for a total of 32 weeks. Placebo: Placebo pill that will match the treatment pill | 0 | 1 | 0 | 1 |
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| D052801 |
| Male Urogenital Diseases |