Evaluation of Healing at Three Time Intervals and Potential for Spontaneous Detachment

Male Circumcision Clinical Trial

Official title:

Evaluation of Healing at Three Time Intervals and Potential for Spontaneous Detachment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01247844
• Other study ID #: 10214
• Status: Completed
• Phase: N/A
• First received: September 7, 2010
• Last updated: March 4, 2015
• Start date: September 2010
• Est. completion date: January 2011

Study information

• Verified date: March 2015
• Source: FHI 360
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review BoardKenya: National Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The objective of this research study is to evaluate the safety and acceptability of the Shang Ring method of medical male circumcision. The Shang Ring is a new circumcision device with a potential role in the safe and cost-effective delivery of circumcision services. The device, developed in China, consists of two concentric plastic rings. Following a ring penile block, the smaller ring is fitted at the base of the coronal sulcus. The foreskin is everted over the inner ring and the larger outer ring is secured over the inner ring. The foreskin is excised and several nicks are made on the incision line to prevent formation of a constricting, circumferential scab. No suturing is required.

In this study, the investigators will evaluate wound healing of men randomized to removal of the Shang Ring at one of three different points in time (Days 7, 14 or 21). Leaving the device on for 14 or 21 days constitutes extended wear of the device.

Sites: Homa Bay District Hospital, Nyanza Province, Kenya

Description:

The objective of this research study is to evaluate the safety and acceptability of the Shang Ring method of medical male circumcision. The Shang Ring is a new circumcision device with a potential role in the safe and cost-effective delivery of circumcision services. The device, developed in China, consists of two concentric plastic rings. Following a ring penile block, the smaller ring is fitted at the base of the coronal sulcus. The foreskin is everted over the inner ring and the larger outer ring is secured over the inner ring. The foreskin is excised and several nicks are made on the incision line to prevent formation of a constricting, circumferential scab. No suturing is required.

In this study, we will evaluate wound healing of men randomized to removal of the Shang Ring at one of three different points in time (Days 7, 14 or 21). Leaving the device on for 14 or 21 days constitutes extended wear of the device.

Although male circumcision has a demonstrated protective effect against HIV transmission, currently available surgical techniques and devices have limitations for widespread deployment in resource-poor areas. High costs and scarcity of trained providers hinder access to male circumcision services in resource-poor areas. Its simple design sets the Shang Ring apart from other male circumcision techniques. The Shang Ring has the potential for safe, effective and inexpensive delivery of male circumcision by trained healthcare personnel in HIV endemic countries.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: January 2011
• Est. primary completion date: January 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 54 Years

Eligibility

Inclusion Criteria:

• Must be aged 18 and 54 years;

• Must be uncircumcised (on examination);

• Must be in good general health;

• Must be HIV sero-negative, with documentation of testing no mor than one week before the procedure;

• Must be free of genital ulcerations or other visible signs of sexually transmissible infections(STI) on examination;

• Must be able to understand study procedures and requirements of study participation;

• Must agree to return to the healthcare facility for the full schedule of follow-up visits after his circumcision;

• Must freely consent to participate in the study and sign a written informed consent form;

• Must have a cell phone or access to a cell phone; and,

• Must agree to provide the study staff with an address, phone number, or other locator information while participating in the research study.

Exclusion Criteria:

• Has a known allergy or sensitivity to lidocaine or other local anesthesia;

• Takes a medication that would be a contraindication for elective surgery, such as an anticoagulant or steroid;

• Has an active genital infection, anatomic abnormality or other condition, which in the opinion of the surgeon, prevents the man from undergoing a circumcision;

• Has known bleeding/clotting disorder (e.g. hemophilia); and,

• Has thalassemia (an inherited autosomal recessive blood disease).

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Male Circumcision

Intervention

Device:
• Shang Ring
The Shang Ring is a sterile device consisting of two concentric medical grade plastic rings: an inner ring with a silicone band and an outer, hinged ring. The inner ring fits inside the outer ring which will lock when snapped together. The Shang Ring comes in multiple sizes. The appropriate size is determined through use of a measuring strip. The man must return to the clinic for device removal. To remove the device, the outer ring locking mechanism is broken open using a tool that is similar to a scalpel handle. Then, a pair of special scissors, specifically designed for this purpose, is used to remove the inner ring after healing

Locations

Country	Name	City	State
Kenya	Homa Bay District Hospital	Homa Bay	Nyanza

Sponsors (5)

Lead Sponsor	Collaborator
FHI 360	Cornell University, EngenderHealth, Kenya National AIDS & STI Control Programme, Ministry of Medical Services, Kenya

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Asses healing time	Assess healing time from date of circumcision	six weeks	Yes
Primary	spontaneous detachment of device	Spontaneous detachment from date of circumcision to three weeks post procedure	21 days	Yes