Monster Screw System Post-Market Clinical Follow-Up Study

Paragon 28

Status: Completed

Conditions: Foot Injury; Ankle Injuries

Treatments: Device: Monster Screw System

Study type: Observational

Funder types: Industry

Identifiers

NCT05190159

P20-SP-0001

Details and patient eligibility

About

Post-market clinical follow-up study on the Monster Screw System

Full description

Ambispective, multi-surgeon, single site, consecutive case series to determine the safety, performance, and benefits of the Monster Screw System.

Enrollment: 82 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• The subject has undergone a foot and/or ankle procedure using the Monster Screw System and completed by one of the investigators.
• The subject has adequate radiographic and medical records

For the Prospective Data Collection:

• The subject is willing to provide written informed consent

Exclusion criteria

-None

Trial design

82 participants in 1 patient group

Monster Screw System

Treatment:

Device: Monster Screw System