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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, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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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.

Primary Outcome

The peak ankle dorsiflexion is the peak ankle backward flexion or bending when walking.

Interventions

  • DEVICE Fiberglass Composite foot
  • DEVICE Carbon Fiber Composite Foot

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2015-06
Est. Completion 2016-05
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT02542761 record still lists

NCT02542761 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Fiberglass Composite foot is the first listed.

NCT02542761 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT02542761's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02542761, the US trial registry maintained by the National Library of Medicine. NCT02542761 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.