Trials / Completed
CompletedNCT05190159
Monster Screw System Post-Market Clinical Follow-Up Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 82 (actual)
- Sponsor
- Paragon 28 · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Post-market clinical follow-up study on the Monster Screw System
Detailed description
Ambispective, multi-surgeon, single site, consecutive case series to determine the safety, performance, and benefits of the Monster Screw System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Monster Screw System | Subjects who have undergone a foot and/or ankle procedure involving the index device |
Timeline
- Start date
- 2022-01-26
- Primary completion
- 2022-09-14
- Completion
- 2022-09-21
- First posted
- 2022-01-13
- Last updated
- 2022-09-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05190159. Inclusion in this directory is not an endorsement.