Monster Screw System Post-Market Clinical Follow-Up Study

NCT05190159 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82

Last updated 2022-09-23

No results posted yet for this study

Summary

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

Conditions

  • Ankle Injuries
  • Foot Injury

Interventions

DEVICE

Monster Screw System

Subjects who have undergone a foot and/or ankle procedure involving the index device

Sponsors & Collaborators

  • Paragon 28

    lead INDUSTRY

Principal Investigators

  • Jacy Legue · Paragon 28

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-26
Primary Completion
2022-09-14
Completion
2022-09-21
FDA Device
Yes

Countries

  • United States

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 NCT05190159 on ClinicalTrials.gov