Robotic MIS With Dexter

Last updated: February 18, 2025
Sponsor: Distalmotion SA
Overall Status: Completed

Phase

N/A

Condition

N/A

Treatment

robotic-assisted surgery

Clinical Study ID

NCT05537727
2021-01
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to confirm the perioperative and early postoperative safety and clinical performance of the Dexter Robotic System (Dexter Surgical System, Model DM-L6).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Aged ≥ 18 years

  • Patient agrees to perform the 30-day follow-up assessment

  • Able to provide signed Informed Consent, according to local regulation

Exclusion

Exclusion Criteria:

  • Morbidly obese patients.

  • Any and all relative and absolute contraindications to endoscopic surgical techniqueapplicable to the use of conventional endoscopic surgical instruments.

  • Bleeding diathesis.

  • Pregnancy.

  • Patients with pacemakers or internal defibrillators.

  • Any planned concomitant procedures.

  • Patient deprived of liberty by administrative or judicial decision or under legalguardianship.

  • Participation in another interventional clinical trial.

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: robotic-assisted surgery
Phase:
Study Start date:
September 27, 2022
Estimated Completion Date:
January 09, 2025

Connect with a study center

  • Hopital Paris Saint-Joseph

    Paris,
    France

    Site Not Available

  • Centre Hospitalier de Saintes

    Saintes,
    France

    Site Not Available

  • UKSH

    Kiel, 24105
    Germany

    Site Not Available

  • Inselspital

    Bern, 3010
    Switzerland

    Site Not Available

  • CHUV

    Lausanne, 1011
    Switzerland

    Site Not Available

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