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MANTIS Endoscopic Clipping Study

NCT05653843 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2025-08-12

Study results available
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Summary

This study is intended to document procedural and clinical effectiveness in consecutive cases in which at least one MANTIS clip is selected, pertaining to use of a new endoscopic clipping device MANTIS™ including but not limited to hemostasis, closure, anchoring and marking.

Conditions

  • Hemostasis
  • Perforation Colon
  • Feeding Tube Complication
  • Endoscopy

Interventions

DEVICE

Endoscopic clip placement in the gastrointestinal tract.

The placement of a mechanical endoscopic clip in the gastrointestinal tract.

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Daniel von Renteln, MD · Centre hospitalier de l'Université de Montréal (CHUM)

  • Jeff Mosko, MD · Unity Health Toronto

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-28
Primary Completion
2024-08-07
Completion
2024-08-07
FDA Device
Yes

Countries

  • United States
  • Canada
  • China
  • Hong Kong
  • India
  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05653843 on ClinicalTrials.gov