Clinical trial

Safety and Acceptability Study of PrePex Device When Removing the Foreskin Shortly After Placement of Device

NCT03132285

Study summary

ClinicalTrials.gov

Safety and Acceptability Study of PrePex Device When Removing the Foreskin Shortly After Placement of Device

Design: INTERVENTIONAL · Status: COMPLETED · Phase: NA

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Drugs and interventions used in this trial

1 registered

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DEVICE · Unmapped registry intervention PrePex Find medicine records · Find other trials using this name

StatusCOMPLETED

Study typeINTERVENTIONAL

Start date2017-03-11

PhaseNA

Conditions

HIV Preventionunresolved

Interventions

PrePexDEVICE

Sponsors & collaborators

Ministry of Health, Zambialead sponsor

Registry source

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Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.