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Clinical trialNCT06572163CompletedInterventional

Clinical Validation Study of the Eximis CS (Contained Segmentation) System

SponsorEximis SurgicalEnrollment23Laparoscopic Gynecological Surgical Procedures
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to evaluate device safety and effectiveness of the Eximis CS System.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Advent Health, 410 Celebration Place

    Celebration, Florida, United States

  • Rosemark Womens Care Specialists

    Idaho Falls, Idaho, United States

  • Maimonides Medical Center

    Brooklyn, New York, United States

  • Oregon Health and Science University School of Medicine

    Portland, Oregon, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
20 Sept 2024
Primary completion
1 Sept 2025
Completion
25 Oct 2025
Last update posted
30 Oct 2025
Registered enrollment
23
Registry id
NCT06572163

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.