MIRA Registry Study

N/AEnrolling By InvitationNCT06856707

Virtual Incision Corporation100 enrolled

Overview

The purpose of the MIRA Surgical System Registry is to accumulate and evaluate real world evidence experience as part of post-market surveillance using the MIRA Surgical System. The studies primary goals are to: * To evaluate the performance of the MIRA Surgical System * To evaluate the Device Safety profile

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Colon Procedures Bowel Resection

Interventions

Use of the MIRA Surgical System during surgeryDEVICE

Use of the MIRA Surgical System to perform robotically assisted colorectal surgery.

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Patients undergoing surgery using the MIRA Surgical System * Subject is able to provide informed consent * Subject is available for post operative follow up visit through 30 days Exclusion Criteria: * Has or is participating in another clinical trial which may confound study results * In the opinion of the investigator, patient is not likely to complete post-operative care and/or return for standard follow-up.

Locations (1)

Bryan Medical Center

Lincoln, Nebraska, United States

Outcomes

Primary Outcomes

Performance of MIRA Surgical System

Successful completion of the surgical procedure using the MIRA Surgical System without conversion to open surgery (Yes/No).

Time frame: From time of procedure through completion of the surgical procedure

Device Safety

Incidence of Device related adverse events and Unanticipated Device Effects

Time frame: From time of surgery using the MIRA Surgical System through 30 days following surgical procedure

Data from ClinicalTrials.gov

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