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Feasibility, Acceptability, and Safety of Neonatal Male Circumcision in Lusaka, Zambia

Feasibility, Acceptability, and Safety of Neonatal Male Circumcision at the University Teaching Hospital in Lusaka, Zambia and in the Lusaka District in Zambia Using Gomco; Plastibell; and Mogen Methods

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01115335
Enrollment
661
Registered
2010-05-04
Start date
2009-10-31
Completion date
2012-01-31
Last updated
2012-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal Male Circumcision

Keywords

neonatal male circumcision, Gomco, Plastibell, Mogen, Safety, Uptake, Acceptability, Feasibility, Zambia

Brief summary

In this study of neonatal male circumcision (NMC), the investigators will examine acceptability of among parents, feasibility of training providers and implementing services in various clinical settings, and the safety of service provision comparing three different surgical methods: the Gomco; the Plastibell; and the Mogen clamp. This operational study is being conducted to inform the scale up of neonatal male circumcision in Zambia.

Detailed description

As male circumcision becomes one component of Zambia's plan to prevent the spread of HIV, it is important to understand the acceptability, feasibility, and safety of implementing NMC services in various clinical settings. In this study, we will examine the acceptability of neonatal male circumcision among parents in several ways. First, we will administer a structured questionnaire on NMC to 1000 consenting parents of newborn boys at a tertiary care institution and 1-2 primary care clinics in Lusaka. All parents approached, regardless of whether or not they complete the survey, will also be offered an opportunity to have their sons circumcised. Uptake will be calculated as the percent of parents approached who consent for their sons to be circumcised. Finally, we will assess parental satisfaction with results of the procedure. To examine the feasibility of training providers and implementing neonatal male circumcision services in various clinical settings, we will train a group of 15-20 health care providers in three different circumcision methods (Gomco clamp, Mogen clamp, and Plastibell) at 2-3 study sites. We will recruit 600 infants to be circumcised during the training. We will use structured questionnaires and skill assessments to evaluate provider competence after completing the training curriculum, provider preferences among the three circumcision methods, and opinion about how NMC should be scaled up within the existing health care system. We will also document logistical difficulties of scaling up NMC services at the study sites. Finally, we will examine the safety of implementing NMC by collecting and analyzing data on complications resulting from the different circumcision methods.

Interventions

PROCEDURENeonatal male circumcision

Circumcision performed on a male infant within the first month of life, using one of 3 devices

Sponsors

University Teaching Hospital, Lusaka, Zambia
CollaboratorOTHER
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
No minimum to 28 Days
Healthy volunteers
Yes

Inclusion criteria

* Male infants who are in the first day of life (including infants \< 24 hours old) and up to 4 weeks of age will be considered for circumcision * Gestational age \>37 weeks at birth

Exclusion criteria

* Any current illness * Bleeding diathesis or family history of bleeding disorder * Abnormality of urethra or penile shaft such as hypospadias * Local infection defined as redness, swelling, or a purulent discharge from the infant penis * Greater than four weeks of age

Design outcomes

Primary

MeasureTime frameDescription
Complication Rate0-6 weeks after the circumcision procedureIncludes intra-operative and post-operative complications such as bleeding, infection, and cosmetic problems

Secondary

MeasureTime frameDescription
Uptake of NMCOngoing, over the course of the study (1.5 years)Defined as % of parents of newborn boys approached during recruitment who consent to having their sons cirucumcised
Provider PreferencesUpon completion of training in NMCMeasure of provider preferences among 3 circumcision devices being compared
Parent Satisfaction6 weeks following the circumcision procedureScore, between 0 and 100, of each parent's satisfaction with the outcome of the NMC procedure

Countries

Zambia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026