MIRA Registry Study

Virtual Incision Corporation

Status: Invitation-only

Conditions: Colon Procedures; Bowel Resection

Treatments: Device: Use of the MIRA Surgical System during surgery

Study type: Observational

Funder types: Industry

Identifiers

NCT06856707

110-002103

Details and patient eligibility

About

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

Enrollment: 100 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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.

Trial design

100 participants in 1 patient group

Surgical

Description:

Patients undergoing surgery with the MIRA Surgical System

Treatment:

Device: Use of the MIRA Surgical System during surgery