Last reviewed · How we verify

NCT03912649: REVALID03

Investigation to Evaluate Performance and Safety of RemovAid ™ in Removal of Contraceptive Implants

Terminated NA Last updated 3 February 2021
What this trial tests

NA trial testing RemovAid in Removal Contraceptive Implant in 15 participants. Terminated before completion.

Timeline
11 June 2019
Primary endpoint
18 November 2020
18 November 2020

Quick facts

Lead sponsorRemovAid AS
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment15
Start date11 June 2019
Primary completion18 November 2020
Estimated completion18 November 2020
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

RemovAid AS

Who can join

Adults 18 to 99, female only, with Removal Contraceptive Implant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The safety and efficacy of a subdermal implant retrieval device (RemovAid) is investigated in a population of 25 women seeking removal of their palpable contraceptive implants. The primary endpoint of the device is to evaluate the performance of the device, specifically its success rate in removing palpable contraceptive implants. The device shall be able to fixate at least 80% of palpable implants, and successfully remove at least 90% of these implants.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other RemovAid AS trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03912649.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing