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Robotic MIS With Dexter

D

Distalmotion

Status

Completed

Conditions

Right Colectomy
Partial Nephrectomy
Hysterectomy

Treatments

Device: robotic-assisted surgery

Study type

Observational

Funder types

Industry

Identifiers

NCT05537727
2021-01

Details and patient eligibility

About

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).

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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 criteria

  • Morbidly obese patients.
  • Any and all relative and absolute contraindications to endoscopic surgical technique applicable 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 legal guardianship.
  • Participation in another interventional clinical trial.

Trial contacts and locations

5

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Central trial contact

Pascal Lehmann

Data sourced from clinicaltrials.gov

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