Triton 1.5 Robotic System for Diagnostic Colonoscopy
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorNeptune Medical
About this trial
This study is a prospective, single-arm, non-randomized, single-site study, focused on evaluating the safety and efficacy of the Triton 1.5 System in diagnostic and basic therapeutic colonoscopy.
Eligibility criteria
Qualifiers
Age ≥ 22 years
Adults indicated for elective screening, surveillance or diagnostic colonoscopy
Subject is willing and able to provide written informed consent prior to receiving any non-standard of care protocol specific procedures
Subject is willing and able to comply with all protocol required preparation and follow- up visits
Disqualifiers
Any medical or physical condition/limitation that would contraindicate a conventional colonoscopy. This assessment will be made by the investigator.
Any active or magnetic implantable medical devices (e.g., pacemakers, defibrillators)
Previous failed colonoscopy (except for inadequate bowel preparation)
BMI > 45 kg/m2
Trial design
Treatments tested in this trial
- Diagnostic Test: Diagnostic Colonoscopy
Treatment groups
40 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov