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Completed Not applicable Interventional

Transtibial Amputation Outcomes Study

ClinicalTrials.gov ID: NCT01821976

Public ClinicalTrials.gov record NCT01821976. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 12:02 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Transtibial Amputation Outcomes Study (TAOS): Comparing Transtibial Amputation With (Ertl) and Without a Tibia-fibula Synostosis Procedure

Study identification

NCT ID
NCT01821976
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Major Extremity Trauma Research Consortium
Other
Enrollment
199 participants

Conditions and interventions

Interventions

  • Ertl Procedure Procedure
  • Burgess Procedure Procedure

Procedure

Eligibility (public fields only)

Age range
18 Years to 60 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2013
Primary completion
Feb 29, 2020
Completion
Feb 29, 2020
Last update posted
May 25, 2026

2013 – 2020

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
22
Facility City State ZIP Site status
University of California San Francisco Medical Center San Francisco California 94143
University of Miami Ryder Trauma Center Miami Florida 33136
Florida Orthopaedic Institute- Tampa General Hospital Tampa Florida 33606
Emory University School of Medicine Atlanta Georgia 30303
Eskenazi Health Indianapolis Indiana 46202
University of Iowa Hospitals & Clinics Iowa City Iowa 52242
University of Maryland/R Adams Cowley Shock Trauma Medical Center Baltimore Maryland 212101
Walter Reed National Military Medical Center Bethesda Maryland 20889
Hennepin County Medical Center Minneapolis Minnesota 55430
University of Mississippi Medical Center Jackson Mississippi 39216
Barnes Jewish Hospital St Louis Missouri 63110
St. Louis University Medical Center St Louis Missouri 63110
Carolinas Medical Center Charlotte North Carolina 28232
Wake Forest University Baptist Medical Center Winston-Salem North Carolina 27157
MetroHealth Medical Center Cleveland Ohio 44109
University of Oklahoma Oklahoma City Oklahoma 73104
Penn State University M.S. Hershey Medical Center Hershey Pennsylvania 17033
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15219
Rhode Island Hospital, Brown University Providence Rhode Island 02903
Vanderbilt University Medical Center Nashville Tennessee 37232
San Antonio Miliary Medical Center Fort Sam Houston Texas 78234-6315
UT Health: The University of Texas Health Science Center at Houston Medical School Houston Texas 77030
University of Wisconsin School of Medicine and Public Health Madison Wisconsin 53726

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01821976, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 25, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01821976 live on ClinicalTrials.gov.

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