Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02542761 · ClinicalTrials.gov registry record · NA
Comparative Performance of Dynamic Elastic Response Feet
A NA study, sponsored by Mayo Clinic.
- Completed
- Registry status
- NA
- Development phase
- 10
- Enrollment target
NCT02542761: Completed NA study, sponsored by Mayo Clinic.
NCT02542761 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 10 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02542761, a NA study, has completed, sponsored by Mayo Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
Study Summary
The purpose of this study was to compare the functional performance of individuals with transtibial amputation using two types of prosthetic foot designs: carbon fiber vs. fiberglass composite.
Interventions
- DEVICE Fiberglass Composite foot
- DEVICE Carbon Fiber Composite Foot
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2015-06 |
| Est. Completion | 2016-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02542761
The ClinicalTrials.gov registry entry for NCT02542761 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Fiberglass Composite foot is the first listed.
NCT02542761 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02542761 about?
NCT02542761 is a clinical study titled "Comparative Performance of Dynamic Elastic Response Feet". The purpose of this study was to compare the functional performance of individuals with transtibial amputation using two types of prosthetic foot designs: carbon fiber vs. fiberglass composite.
What is the current status of trial NCT02542761?
This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2015-06. Estimated completion is 2016-05.
What interventions are being tested in trial NCT02542761?
The interventions under investigation include: Fiberglass Composite foot (DEVICE), Carbon Fiber Composite Foot (DEVICE).
Who is sponsoring clinical trial NCT02542761?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.