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NCT Number: NCT01891409

Use of the Shang Ring Circumcision Device in Boys Below 18 Years Old in Kenya

A proof of concept study to evaluate the feasibility of using the Shang Ring, a novel male circumcision device across all childhood age groups namely infants (under 1), 1-5 age group, 6-12 age group and the 13-17 age group. The study will evaluate the safety, efficacy and course of wound healing when using the Shang Ring technique across the four childhood age groups.

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Key information

About this study

A proof of concept study to evaluate the feasibility of using the Shang Ring, a novel male circumcision device across all childhood age groups namely infants (under 1), 1-5 age group, 6-12 age group and the 13-17 age group. The study will evaluate efficacy, procedure time, difficulties during surgery and post-operative events shall be assessed. To evaluate safety, the investigators will clinically observe for adverse events during the course of healing. The investigators will also evaluate to length of time taken for complete healing to be achieved.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be accompanied by the parent or legally acceptable representative (LAR), who freely consents for participation of the child into the study;
  • Assent from participant 7 years of age and above who understand study procedure;
  • Aged between 1 month and 17 years(inclusive);
  • Body weight of more than 2.5 kgs and penile shaft more than 1 cm in length.
  • Must be in good general health;
  • Must be free of genital ulcerations or other visible signs of STI (on examination);
  • Parent or LAR and if possible the client must be able to understand study procedures and requirements of study participation;
  • Parent or LAR must agree to return the client to the study site for the full schedule of follow-up visits after his circumcision;
  • Parent or LAR must have a cell phone or access to a cell phone; and,
  • Parent or LAR 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 known bleeding/clotting disorder (e.g. hemophilia);
  • Has any congenital genitourinary abnormality;
  • Has an active genital infection, anatomic abnormality or other condition (e.g. severe obesity, diabetes or sickle cell anemia), which in the opinion of the surgeon, prevents the man from undergoing a circumcision as part of this study; or
  • Is currently participating in another biomedical research study.

Treatment and study plan

Male circumcision using the Shang Ring device

Device

Other names: Shang ring male circumcision device

Primary outcomes

  1. To evaluate safety when using the Shang Ring technique across the 4 age groups ranging from infants to adolescents.

    Time frame: 42 days after circumcision

    Documentation of adverse events based on clinical exam findings

Secondary outcomes

  1. To evaluate efficacy when using the Shang Ring technique across the 4 age groups ranging from infants to adolescents.

    Time frame: 42 days after circumcision

    To evaluate efficacy, procedure time, peri- and postoperative surgical complications, and problems with use of the device will be assessed.

  2. To evaluate the course of wound healing when using the Shang Ring technique across the 4 age groups ranging from infants to adolescents.

    Time frame: 42 days after circumcision

    Evaluation of the course of healing and length of time required for complete healing will be based on clinical exam findings.

  3. To determine the acceptability of the Shang Ring device by the participants (or their parents)

    Time frame: 42 days after circumcison

    Clients and/or parents shall be interviewed on their experience with the Shang Ring during their participation in the study.

  4. To evaluate the ease of use of the Shang Ring technique across the 4 age groups ranging from infants to adolescents

    Time frame: 42 days after circumcision

    To evaluate the ease of use of the Shang Ring device, clinicians shall be interviewed on the difficulties they faced with using the device and their perception about use of the device relative to conventional surgical approaches

Sponsors and collaborators

Lead sponsor

EngenderHealth

Other

Collaborators

  • Kenya Ministry of Health
  • Kenya National AIDS & STI Control Programme
  • Weill Medical College of Cornell University

Registry information

Official study title

Use of the Shang Ring Device in All Four Childhood Age Groups in the African Population

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jul 3, 2013
Registry last updated
Jan 19, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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