Male Circumcision Clinical Trial
Official title:
One-Arm, Open Label, Prospective Safety Study of the PrePex Device for Non-Surgical Adult Male Circumcision During Phased in National Implementation in an Effort to Prevent the Spread of HIV.
It is well known from a range of observational and epidemiological studies that the lifetime
risk of acquiring HIV among males can be significantly reduced via circumcision. Numerous
papers on the topic were published in the past two decades to elevate HIV prevention
awareness, especially in sub-Saharan countries.
Rwanda has a national plan to offer a voluntary circumcision program to 2 million adult men
in 2 years as part of a comprehensive HIV prevention package. To achieve this goal, the
government is continuing to study the PrePex™ device, developed to enable rapid adult male
circumcision in resource limited settings.
In February 2012, Rwanda has received WHO recommendation to scale up Adult Male male
circumcision (MC) using the PrePex device. Based on WHO recommendation (Use of devices for
adult male circumcision in public health HIV prevention programs: Conclusions of the
Technical Advisory Group on Innovations in Male Circumcision, March 2012, WHO/HIV/2012.7),
which recommended that the phased implementation include an active surveillance of the first
1000 clients to identify and record all adverse events and side-effects based on
standardized definitions. The active surveillance may change to passive surveillance after
the first 1000 clients, if the incidence of events is reassuringly low, as determined by
independent review.
Male circumcision can reduce the lifetime risk of HIV infection by 60% in high risk areas
such as Sub Saharan Africa. In 2009, the US Government (USAID) reported that scaling up male
circumcision to reach 80 percent of adult and newborn males in 14 African countries by 2015
could potentially avert more than 4 million adult HIV infections between 2009 and 2025 and
yield annual cost savings of US$1.4 - 1.8 billion after 2015, with a total net savings of
US$20.2 billion between 2009 and 2025.
There are over 38 million adolescent and adult males in Africa that could benefit from male
circumcision for HIV prevention. The challenge Africa faces is how to safely scale up a
surgical procedure in resources limited settings.
The government of Rwanda has a national plan to decrease the incidence rate of HIV by 50%,
and to support this, needs to conduct 2 million voluntary adult male circumcisions in 2
years, a nearly impossible goal with surgical methods. Hence, the government embarked upon a
pre-safety and pivotal study to test The PrePex™ device, a new device and methodology for
rapid adult male circumcision in resource limited settings.
;
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01247844 -
Evaluation of Healing at Three Time Intervals and Potential for Spontaneous Detachment
|
N/A | |
Completed |
NCT02242565 -
Safety and Effectiveness of Different ShangRing Device Sizes for Adult Male Circumcision in Lusaka, Zambia
|
N/A | |
Completed |
NCT00993811 -
The Shang Ring: A Novel Male Circumcision Device for HIV Prevention
|
Phase 1 | |
Completed |
NCT02281435 -
Follow Up Study to Evaluate a Non-Surgical Device for Adult Male Circumcision for Screen Failure Subjects
|
N/A | |
Completed |
NCT04263064 -
High Volume Caudal Study
|
Early Phase 1 | |
Completed |
NCT02091726 -
Phase 4 Field Trial of the Unicirc Instrument With Tissue Adhesive
|
N/A | |
Completed |
NCT02309710 -
Male Circumcision (MC) Using the ShangRing™ Device in Malawi
|
Phase 1 | |
Completed |
NCT02167776 -
From Obstacles to Opportunities for Male Circumcision in Tanzania
|
N/A | |
Completed |
NCT01150370 -
A Pivotal Study to Assess the Safety and Efficacy of The PrePex System, a Male Circumcision Device and Methodology for Rapid Scale up of Painless and Bloodless National Circumcision Programs, in Urban and Remote Rural Settings
|
N/A | |
Completed |
NCT01434628 -
Cohort Field Study to Assess the Safety and Efficacy of the PrePex Device for Non-Surgical Circumcision When Performed by Nurses
|
N/A | |
Active, not recruiting |
NCT03914365 -
Pudendal Nerve Block vs Penile Nerve Block for Analgesia During Pediatric Circumcision
|
N/A | |
Completed |
NCT03634358 -
Bipolar Scissors for Circumcision
|
N/A | |
Completed |
NCT02277795 -
Evaluation of the AccuCirc for Early Infant Male Circumcision in Nyanza, Kenya
|
N/A | |
Completed |
NCT01567436 -
A Prospective Field Study: Introducing the Shang Ring in Routine Clinical Settings
|
Phase 4 | |
Completed |
NCT03223532 -
Randomized Trial Comparing PrePex Day 7 Foreskin Removal Procedure (FRP) to a Day 0 PrePex FRP .
|
N/A |