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临床试验/NCT03223532
NCT03223532已完成不适用

A Prospective, Randomized, Open Label Trial Comparing PrePex™ Day 7 Foreskin Removal Procedure (FRP) to a PrePex Day 0 FRP of Male Circumcision in Resource Limited Settings

Nyanza Reproductive Health Society2 个研究点 分布在 1 个国家目标入组 152 人开始时间: 2017年4月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
152
试验地点
2
主要终点
Incidence of Serious Adverse Events related to the Day 0 FRP

研究概览

简要总结

A Prospective, Randomized, Open Label Trial Comparing PrePex™ Day 7 (FRP) to a PrePex Day 0 FRP of Male Circumcision in Resource Limited Settings.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
13 Years 至 49 Years(Child, Adult)
性别
Male
接受健康志愿者

入选标准

  • Ages - 13 to 49 years
  • Uncircumcised
  • Adequately vaccinated, or willing to be vaccinated, against Tetanus based on appropriate national guidance for male circumcision
  • Willing to be circumcised
  • Legal guardian consent to the procedure for ages 13-18 years
  • Agrees to be circumcised by any of the study methods, Day0 FRP or Day7 FRP as will be determined randomly
  • Able to understand the study procedures and requirements
  • Agrees to abstain from sexual intercourse for 8 weeks after circumcision
  • Agrees to abstain from masturbation for at least 2 weeks after Removal
  • Agrees to return to the health care facility for follow-up visits (or as instructed) after his circumcision for a period of 6 weeks post removal (7 weeks total)
  • Subject able to comprehend and freely give informed consent for participation in this study and is considered by the investigator to have good compliance for the study

排除标准

  • Legal guardian withholds consent for ages 13-18 years
  • Active genital infection, anatomic abnormality or other condition, which in the opinion of the investigator prevents the subject from undergoing a circumcision
  • Subject with the following diseases/conditions: phimosis, paraphimosis, adhesions, warts under the prepuce, torn or tight frenulum, narrow prepuce, hypospadias, epispadias
  • Known bleeding / coagulation abnormality, uncontrolled diabetes
  • Subject that to the opinion of the investigator is not a good candidate
  • Subject does not agree to anonymous video and photographs of the procedure and follow up visits.

研究组 & 干预措施

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

干预措施: PrePex Day 7 FRP (Device)

PrePex Day 0 FRP

Experimental

On the day of device placement the foreskin is removed, the device is removed 1 week later.

干预措施: PrePex Day 0 FRP (Device)

结局指标

主要结局

Incidence of Serious Adverse Events related to the Day 0 FRP

时间窗: 8 weeks

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.

次要结局

  • Acceptability of PrePex Day 0 FRP(8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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