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Clinical Trial Summary

This randomized trial will compare different approaches to removing a subdermal contraceptive implant from the upper arm of 225 women in Uganda. The experimental approach is a hand-held device (RemovAid) that incises the skin and grasps the implant for extraction. Safety and efficacy endpoints will be compared to the traditional removal approach (scalpel, forceps, tweezers).


Clinical Trial Description

The trial assigns participants to one of three arms: RemovAid+lidocaine patch (n=75), RemovAid+lidocaine injection (n=75) or traditional approach+lidocaine injection(n=75). Complication rates in the different arms will be compared. Efficacy (successful implant removal) will be the secondary comparisons. Finally, pain during removal and duration of removal procedure will be compared. Participants will return to the clinic within 4 weeks of the removal procedure to record the healing process and final interventions (if any). ;


Study Design


Related Conditions & MeSH terms

  • Removal of a Contraceptive Subdermal Implant

NCT number NCT04120337
Study type Interventional
Source RemovAid AS
Contact
Status Completed
Phase N/A
Start date December 23, 2019
Completion date April 1, 2021