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Recruiting NCT07123051

Robotic Assisted Right Colectomy With the DEXTER Robotic Surgery System

— Observational Right Colectomy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: right colectomy.
Who it may be relevant to
Registry conditions: Right Colectomy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France, Germany, Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing robotic-assisted right colectomy.

Interventions

  • Device right colectomy
    Robotic-assisted right colectomy with the DEXTER robotic surgery system

Primary outcome measures

  • Primary safety outcome [Time frame: up to 30 days after surgery]
  • Primary efficacy outcome [Time frame: Intraoperative]

Eligibility criteria

Inclusion criteria

  • Aged > 18 years
  • Patient agrees to perform the 30-day follow-up assessment as per standard of care

Exclusion criteria

  • History of radiotherapy on the target surgical area
  • Patients with distant metastasis
  • Any planned concomitant procedures
  • History of major abdominal surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Switzerland · 2 centers
  • Spitäler FMI AG — Interlaken
  • SRO AG Spital Langenthal — Langenthal
France · 1 center
  • CH Châteauroux - Le Blanc — Châteauroux
Germany · 1 center
  • Artemed Klinikum München Süd — Munich

Identifiers

NCT: NCT07123051 · 2025-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗