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NCT02923544 · ClinicalTrials.gov registry record · NA

Trial of YUMI Uterine Manipulator

A NA study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
NA
Development phase
11
Enrollment target

NCT02923544: Completed NA study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT02923544 is a NA study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 11 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02923544, a NA study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

The purpose of this study is to test the feasibility and safety of using a new device called Yukio's Uterine Manipulating Instrument (YUMI). The YUMI is a type of uterine manipulator. It is a reusable metal device designed to be simple and study. It is also adjustable in size which makes it easy for surgeons to use. It will be placed at the beginning of the surgery and removed at the end. This study will allow the researchers to find out if the surgeons find the YUMI effective and easy to use. It will also allow the researchers to see if the device is safe. This is the first time that the YUMI is being used in humans.

Primary Outcome

The YUMI manipulator will be considered successfully placed when the device is inserted into the uterus and secured in place to hold for the duration of the procedure.

Interventions

  • PROCEDURE YUMI manipulator

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2016-09-27
Est. Completion 2022-05-03
Phase NA
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT02923544 record still lists

NCT02923544 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which YUMI manipulator is the first listed.

NCT02923544 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02923544 about?

NCT02923544 is a clinical study titled "Trial of YUMI Uterine Manipulator". The purpose of this study is to test the feasibility and safety of using a new device called Yukio's Uterine Manipulating Instrument (YUMI). The YUMI is a type of uterine manipulator. It is a reusable metal device designed to be simple and study. It is also adjustable in size which makes it easy for...

What is the current status of trial NCT02923544?

This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2016-09-27. Estimated completion is 2022-05-03.

What interventions are being tested in trial NCT02923544?

The interventions under investigation include: YUMI manipulator (PROCEDURE).

Who is sponsoring clinical trial NCT02923544?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02923544's enrollment target sits among peer trials

11 1927th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02923544, the US trial registry maintained by the National Library of Medicine. NCT02923544 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.