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COMPLETED NA

Prosthetic Socket Interface Design on Socket Comfort, Residual Limb Health, and Function for the Transfemoral Amputee

NCT02773056 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this clinical trial is to determine if the Dynamic Socket and Sub-Ischial alternative interface designs improve socket comfort, residual limb health, increase function and be preferred over the standard of care Ischial Ramus Containment (IRC) interface for the military and veteran living with transfemoral limb loss.

Conditions Studied

Interventions

  • DEVICE Ischial Ramus Containment (IRC)
  • DEVICE Dynamic Socket Ischial Ramus Containment (IRC)
  • DEVICE Sub-Ischial Interface (Sub-I)

Study Locations (1)

Florida

  • University of South Florida — Tampa

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2016-06
Est. Completion 2018-03-30
Phase NA

Sponsor

University of South Florida

144 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02773056

The ClinicalTrials.gov registry entry for NCT02773056 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of South Florida, which has 144 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Amputation appearing as the primary indexed condition, and to 3 interventions — of which Ischial Ramus Containment (IRC) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02773056 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02773056 about?

NCT02773056 is a clinical study titled "Prosthetic Socket Interface Design on Socket Comfort, Residual Limb Health, and Function for the Transfemoral Amputee". The primary objective of this clinical trial is to determine if the Dynamic Socket and Sub-Ischial alternative interface designs improve socket comfort, residual limb health, increase function and be preferred over the standard of care Ischial Ramus Containment (IRC) interface for the military and v...

What is the current status of trial NCT02773056?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2016-06. Estimated completion is 2018-03-30.

What conditions does trial NCT02773056 study?

This clinical trial studies the following conditions: Amputation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02773056?

The interventions under investigation include: Ischial Ramus Containment (IRC) (DEVICE), Dynamic Socket Ischial Ramus Containment (IRC) (DEVICE), Sub-Ischial Interface (Sub-I) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02773056?

This trial is sponsored by University of South Florida, which has 144 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02773056 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial