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| ID | Type | Description | Link |
|---|---|---|---|
| 010-04-14 | Other Identifier | UNZABREC (local IRB) |
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| Name | Class |
|---|---|
| Bill and Melinda Gates Foundation | OTHER |
| Ministry of Health, Zambia | OTHER_GOV |
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The purpose of this study was to assess the safety, effectiveness and acceptability of providing a reduced number of ShangRing sizes for adult voluntary medical male circumcision (VMMC) within routine service delivery in Lusaka, Zambia.
We conducted a randomized controlled trial and enrolled 500 HIV-negative men aged 18-49 years at 3 clinics. Participants were randomized to 1 of 2 study arms (Standard Sizing arm vs Modified Sizing arm) in a 1:1 ratio. All 14 adult ShangRing sizes (40-26 mm inner diameter, each varying by 1 mm) were available in the Standard Sizing arm; the Modified Sizing arm used every other size (40, 38, 36, 34, 32, 30, 28 mm inner diameter). Each participant was scheduled for 2 follow-up visits: the removal visit (day 7 after placement) and the healing check visit (day 42 after placement), when they were evaluated for adverse events (AEs), pain, and healing.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control: all-sizes of ShangRing | Other | All-sizes of ShangRings will be available. |
|
| Reduced-sizes | Active Comparator | 7 adult sizes of ShangRings will be available |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ShangRing | Device | ShangRing device for male circumcision |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percentage and 95% confidence interval of men with at least one moderate or severe adverse event. | To assess the safety of ShangRing procedures when providers choose among 7 adult sizes (reduced-sizes or treatment arm) versus the full range of 14 adult sizes (all-sizes or control arm) during routine service delivery in Lusaka, Zambia. | 42 days |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of men who cannot be properly fitted with a ShangRing device | Assess the effectiveness of ShangRing procedures in the reduced-sizes arm. | 42 days |
| Evaluate the acceptability of ShangRing procedures among participants and providers |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Robert Zulu, MD | University Teaching Hospital | Principal Investigator |
| Paul Feldblum, PhD | FHI 360 | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chilenje Urban Health Centre | Lusaka | Zambia | ||||
| The University Teaching Hospital (UTH) |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27331587 | Result | Feldblum PJ, Zulu R, Linyama D, Long S, Nonde TJ, Lai JJ, Kashitala J, Veena V, Kasonde P. Randomized Controlled Trial of the ShangRing for Adult Medical Male Circumcision: Safety, Effectiveness, and Acceptability of Using 7 Versus 14 Device Sizes. J Acquir Immune Defic Syndr. 2016 Jun 1;72 Suppl 1(Suppl 1):S30-5. doi: 10.1097/QAI.0000000000001015. |
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Participant acceptability (with procedure and cosmetic appearance), pain, and time to return to normal activity after ShangRing circumcision, overall and in each arm.
Provider acceptability assessing ease, duration, and complications, and preferences comparing ShangRing with other methods of circumcision, and comparing reduced-sizes with all-sizes provision.
| 42 days |
| Percentage of men with complete healing at 42 days | Percentage of men with complete healing at 42 days for all study participants, and within each arm of the trial. | Day 42 |
| Lusaka |
| Zambia |