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Safety and Feasibility of the Use of the Dual Robotic Arm Accessory With the Levita Magnetic Surgical System in Laparoscopic Procedures

NCT05695989 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2025-02-21

Study results available
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Summary

The purpose of this study is to evaluate the safety and feasibility of the Levita Dual Robotic Arm Accessory (DRAA) used with the Levita Magnetic Surgical System (MSS)

Conditions

  • Bariatric Surgery Candidate
  • Cholelithiases
  • Other Disease

Interventions

DEVICE

Dual Robotic Arm Accessory (DRAA)

Dual Robotic Arm Accessory (DRAA)

Sponsors & Collaborators

  • The Cleveland Clinic

    collaborator OTHER

  • Levita Magnetics

    lead INDUSTRY

Principal Investigators

  • Julio Jimenez, MD · Hospital Tisne

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-19
Primary Completion
2023-03-08
Completion
2023-03-08

Countries

  • Chile

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05695989 on ClinicalTrials.gov