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NCT06249126 · ClinicalTrials.gov registry record · NA

Primary Subtalar Arthrodesis for Calcaneal Fractures

A NA study of Calcaneus Fracture, sponsored by Wake Forest University Health Sciences.

Recruiting
Registry status
NA
Development phase
218
Enrollment target
14
Study locations

NCT06249126: Recruiting NA study of Calcaneus Fracture, sponsored by Wake Forest University Health Sciences.

NCT06249126 is a NA study of Calcaneus Fracture that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 218 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (84% lower). The trial reports 14 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06249126, a NA study of Calcaneus Fracture, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.

RECRUITING
Registry status
NA
Development phase
218 participants
Enrollment target
14
Study locations

Study Summary

Management of severe injuries to the heel (displaced intra-articular calcaneus fractures) continues to be a major challenge for orthopedic surgeons. Previous studies have demonstrated poor outcomes, and results show that patients experience long-term pain and decreased quality of life postoperatively. Poor outcomes are driven by pain, in particular, which is linked to post-traumatic subtalar arthritis.

Primary Outcome

The primary outcome is return to work/duty as measured by the International Physical Activity Questionnaire (IPAQ). The IPAQ is a validated, self-report measure that captures detailed information about participation in a wide range of physical activities, including the number of days and amount of time spent in the previous 7 days. Responses for each type of physical activity are then transformed into the number of Metabolic Equivalent for Tasks (METs), and a METs/week is calculated for each pat

Conditions Studied

Interventions

  • PROCEDURE Primary Fusion (Open Reduction Internal Fixation (ORIF) + Primary Subtalar Arthrodesis (PSTA)
  • PROCEDURE Open Reduction Internal Fixation (ORIF) only

Study Locations (14)

North Carolina

  • University of North Carolina Chapel Hill - Chapel Hill
  • Atrium Health Carolinas Medical Center - Charlotte
  • OrthoCarolina Foot and Ankle Institute - Charlotte
  • Atrium Health Cabarrus - Concord
  • Atrium Health Wake Forest Baptist - Winston-Salem

Georgia

  • Emory University, Grady Memorial Research Hospital - Atlanta
  • Atrium Health Navicent - Macon

Kentucky

  • University of Kentucky - Lexington

Louisiana

  • Louisiana State University - University Medical Center New Orleans - New Orleans

Maryland

  • University of Maryland Medical Center - Baltimore

New York

  • NYC Health and Hospital/Bellevue - New York

South Carolina

  • Prisma Health - Greenville

Tennessee

  • Vanderbilt University Medical Center - Nashville

Trial Details

FieldValue
Enrollment Target 218 participants
Start Date 2024-09-02
Est. Completion 2026-12
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What NCT06249126 shows while recruiting

NCT06249126 is an interventional study that assigns participants to a tested intervention. The registered 218 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (84% lower).

The record links to 1 condition, with Calcaneus Fracture appearing as the primary indexed condition, and to 2 interventions - of which Primary Fusion (Open Reduction Internal Fixation (ORIF) + Primary Subtalar Arthrodesis (PSTA) is the first listed.

NCT06249126 lists 14 locations in 9 states (North Carolina, Georgia, Kentucky).

Frequently Asked Questions

What is clinical trial NCT06249126 about?

NCT06249126 is a clinical study titled "Primary Subtalar Arthrodesis for Calcaneal Fractures". Management of severe injuries to the heel (displaced intra-articular calcaneus fractures) continues to be a major challenge for orthopedic surgeons. Previous studies have demonstrated poor outcomes, and results show that patients experience long-term pain and decreased quality of life postoperativel...

What is the current status of trial NCT06249126?

This trial is currently recruiting. It is a NA study. The enrollment target is 218 participants. The study started on 2024-09-02. Estimated completion is 2026-12.

What conditions does trial NCT06249126 study?

This clinical trial studies the following conditions: Calcaneus Fracture.

What interventions are being tested in trial NCT06249126?

The interventions under investigation include: Primary Fusion (Open Reduction Internal Fixation (ORIF) + Primary Subtalar Arthrodesis (PSTA) (PROCEDURE), Open Reduction Internal Fixation (ORIF) only (PROCEDURE).

Who is sponsoring clinical trial NCT06249126?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06249126 being conducted?

This trial has 14 study locations across Georgia, Kentucky, Louisiana, Maryland, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT06249126's enrollment target sits among peer trials

218 485th of 2000 higher than 1,516 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 NCT06249126, the US trial registry maintained by the National Library of Medicine. NCT06249126 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.