Male Circumcision Clinical Trial
— Unicirc003Official title:
Phase 4 Field Trial of the Unicirc Instrument With Tissue Adhesive
NCT number | NCT02091726 |
Other study ID # | Unicirc 003 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2014 |
Est. completion date | September 2014 |
Verified date | September 2018 |
Source | Simunye Primary Health Care |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a field trial of the Unicirc instrument to excise the foreskin, plus use of cyanoacrylate tissue adhesive to seal the wound.
Status | Completed |
Enrollment | 110 |
Est. completion date | September 2014 |
Est. primary completion date | September 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - Men at least 18 years of age Exclusion Criteria: - Poor general health - Anatomical abnormalities that would complicate circumcision - Bleeding disorder - Ongoing infection - Cannot attend followup visits |
Country | Name | City | State |
---|---|---|---|
South Africa | Simunye Primary Healthcare | Cape Town | Western Cape |
Lead Sponsor | Collaborator |
---|---|
Simunye Primary Health Care |
South Africa,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time for Procedure | Intraoperative time, total | 1 hour | |
Secondary | Completely Healed at 4 Weeks | Definition: Completely epithelialized; no superficial ulcerations or granulation tissue present | 4 weeks | |
Secondary | Wound Separation | Wound separation caused by adhesive failure (minor --requires no treatment) | 4 weeks | |
Secondary | Cosmetic Result Excellent | Excellent: scar line straight without any irregularity Irregular: Some irregularity to scar line Scalloped: wavy appearane to scar line | 4 weeks | |
Secondary | Participant Fully Satisfied and Would Recommend to Friends and Family | Yes to both of the following questions: Are you fully satisfied with your circumcision result? Would you recommend circumcision to friends or family? | 4 weeks |
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 |
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 |
NCT01921608 -
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
|
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 |