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A Prospective, Randomized, Open Label Trial Comparing PrePexâ„¢ Day 7 (FRP) to a PrePex Day 0 FRP of Male Circumcision in Resource Limited Settings.
Study Objectives:
To compare the safety and acceptability of PrePex Day 7 Foreskin Removal Procedure (FRP) (herein: PrePex) versus PrePex Day0 FRP
Planned Subjects Population:
One hundred and fifty (150) subjects scheduled for voluntary medical male circumcision. The subjects will be randomly divided into two unbalanced study arms (2:1), Day0 FRP arm which will include hundred (100) subjects and PrePex arm which will include fifty (50) subjects.
Study duration per subject will be up to 7 weeks and will include a total of 9 visits.
Study Site: University of Nairobi, Illinois, and Manatoba (UNIM) Research and Training Centre, Kisumu, Kenya
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PrePex Day 7 FRP | Active Comparator | Standard PrePex procedure, 1 week after device placement foreskin and device are removed. *Subjects must be adequately vaccinated, or willing to be vaccinated, against Tetanus based on appropriate national guidance for male circumcision |
|
| PrePex Day 0 FRP | Experimental | On the day of device placement the foreskin is removed, the device is removed 1 week later. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PrePex Day 7 FRP | Device | Standard PrePex procedure, foreskin and device are removed 1 week after device application. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Serious Adverse Events related to the Day 0 FRP | Assessing the safety of PrePex Day 0 FRP compared to the standard Day 7 FRP, by means of the following parameter: Incidence of Serious Adverse Events. | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Acceptability of PrePex Day 0 FRP | Evaluating the PrePex Day 0 FRP acceptability to subjects and health care providers compared to the standard Day 7 FRP, by means of the following parameters:
|
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Inclusion Criteria:
Exclusion Criteria:
Uncircumcised males willing to undergo the non-surgical PrePex male circumcision procedure
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| Name | Affiliation | Role |
|---|---|---|
| Fredrick Otieno, M.D. | Nyanza Reproductive Health Society | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nyanza Reproductive Health Society | Kisumu | Nyanza | P.O. Box 1764 | Kenya |
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A Prospective, Randomized, Open Label Trial.
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| PrePex Day 0 FRP | Device | Removal of the foreskin shortly after device application, the device is removed 1 week later |
|
| 8 weeks |