Triton 1.5 Robotic System for Diagnostic Colonoscopy

Sponsor
Neptune Medical
Study ID
NCT07606963
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Diagnostic Test: Diagnostic Colonoscopy — DEVICE
    This study will serve to evaluate the safety and efficacy of the Triton 1.5 System for performing diagnostic, screening, surveillance, and basic therapeutic tasks (e.g., polypectomy for lesions ≤2cm).

Study Details

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.

Key Dates

First listed
May 26, 2026
Start date
Aug 1, 2026
Status verified
May 2026
Primary completion
Sep 30, 2026
Completion
Oct 15, 2026

Study Design

Enrollment
40 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Arms

  • Other: Single Arm
    This study is a prospective, single-arm, non-randomized, single-site study, which is deigned to evaluate the safety and efficacy of the Triton 1.5 System for performing diagnostic, screening, surveillance, and basic therapeutic tasks (e.g., polypectomy for lesions ≤2cm) during endoscopic procedures.

Primary Outcome Measure

Primary Safety Endpoint - Incident of Major Adverse Events within 48 Hours [ Time Frame: 48 Hours ]

Central Contacts

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