- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07822698
Sustentaculum Tali Screw Fixation Mode and Postoperative Foot-Ankle Function in Calcaneal Fractures
Impact of Sustentaculum Tali Screw Fixation Mode on Radiographic and Functional Outcomes in Patients With Intra-Articular Calcaneal Fractures: An Ambidirectional Cohort Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Calcaneal fractures account for approximately 1% to 2% of all fractures and are the most common tarsal bone fractures, usually caused by high-energy injuries such as falls from height and motor vehicle accidents. Most are intra-articular fractures involving the subtalar joint. Open reduction and internal fixation is the mainstay of treatment for displaced intra-articular calcaneal fractures, aiming to restore the congruity of the subtalar articular surface and the normal morphology of the calcaneus.
The sustentaculum tali is a bony prominence on the medial side of the calcaneus that forms the middle facet of the subtalar joint. Because of its dense bone and strong ligamentous attachments, it is a key anchor point for fracture reduction and internal fixation. During surgery via a lateral approach, a sustentaculum tali screw is inserted from the lateral wall toward the medial side to provide stable support for the reduced posterior articular surface.
Depending on the screw tip position on postoperative imaging, fixation is classified as sustentaculum tali fixation (ST; screw penetrates within the range of the sustentaculum tali) or sustentaculum tali fragment fixation (STF; screw is fixed into the larger medial fragment containing the sustentaculum tali, with the penetration point outside the sustentaculum tali range). Because the sustentaculum tali is small and irregularly shaped, accurate screw placement is technically demanding, with reported accuracy of only 60% to 80% even among experienced surgeons. Recent studies suggest that fixation into the sustentaculum fragment may achieve clinical outcomes similar to precise sustentaculum tali fixation; however, the effect of the different fixation modes on postoperative foot and ankle function remains insufficiently investigated.
Design and methods: This is an ambidirectional cohort study. Approximately 92 participants with intra-articular calcaneal fractures treated by open reduction and internal fixation will be enrolled, including retrospective cases from January 2015 to August 2026 and prospective cases from September 2026. Participants will be naturally allocated to the ST or STF group according to the fixation mode determined on postoperative lateral and axial X-rays; no randomization is performed and no treatment plan is altered by the study.
Data are collected during routine clinical follow-up at 1 week, 6 weeks, 12 weeks, 24 weeks, and 1 year after surgery; no additional examinations or interventions are required. Radiographic parameters (Böhler's angle, Gissane's angle, calcaneal height and width) are measured on pre- and postoperative X-rays, and functional outcomes are assessed with the AOFAS ankle-hindfoot score and the Maryland Foot Score at least 12 months postoperatively.
Statistical analysis: Continuous variables will be compared using the t-test or the Wilcoxon rank-sum test according to their distribution, and categorical variables will be compared using the chi-square test. Two-sided P < 0.05 will be considered statistically significant. Multivariable regression may be used to adjust for potential confounders where appropriate. Analyses will be performed with SPSS 26.0 (IBM, Armonk, NY, USA).
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Clinical Trial Office
- Phone Number: 010-82266699
- Email: bysy@bjmu.edu.cn
Study Locations
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Beijing Municipality
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Beijing, Beijing Municipality, China, 100191
- Peking University Third Hospital
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Contact:
- Clinical Trial Office
- Phone Number: 010 82266699
- Email: bysy@bjmu.edu.cn
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged ≥ 18 years.
Diagnosis of intra-articular calcaneal fracture.
Treated with open reduction and internal fixation (ORIF).
Availability of postoperative lateral and axial X-rays for assessment of screw tip position.
Complete medical records for retrospective data collection, or willingness to participate in prospective follow-up.
Written informed consent for prospective participants; informed consent waived for retrospective participants as approved by the ethics committee.
Exclusion Criteria:
- Pathological fractures.
Open calcaneal fractures.
Previous surgery on the affected calcaneus.
Severe medical conditions that may affect follow-up or functional assessment.
Inability to complete follow-up or functional questionnaires.
Lack of adequate imaging or medical records for group allocation.
Patients who declined to participate (for prospective cases).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Sustentaculum Tali (ST) Fixation
Participants with intra-articular calcaneal fractures treated with open reduction and internal fixation.
The exposure of interest is screw tip position: the sustentaculum tali screw penetrates within the range of the sustentaculum tali on postoperative lateral and axial X-rays.
No treatment was assigned by the study; all participants received routine clinical care.
|
Postoperative screw tip position on lateral and axial X-rays, classified as either ST (within the sustentaculum tali) or STF (in the larger medial fragment, outside the sustentaculum tali range).
This is the exposure of interest; the study does not assign this exposure.
|
|
Sustentaculum Tali Fragment (STF) Fixation
Participants with intra-articular calcaneal fractures treated with open reduction and internal fixation.
The exposure of interest is screw tip position: the screw is fixed into the larger medial fragment containing the sustentaculum tali, with the penetration point outside the sustentaculum tali range on postoperative lateral and axial X-rays.
No treatment was assigned by the study; all participants received routine clinical care.
|
Postoperative screw tip position on lateral and axial X-rays, classified as either ST (within the sustentaculum tali) or STF (in the larger medial fragment, outside the sustentaculum tali range).
This is the exposure of interest; the study does not assign this exposure.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maryland Foot Score
Time Frame: At least 12 months postoperatively
|
A validated 100-point scoring system for assessing foot function after injury.
Domains include pain, gait, distance walked, stability, support, limp, and wearing shoes.
Higher scores indicate better function.
Score categories: Excellent 90-100; Good 75-89; Fair 50-74; Failure <50.
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At least 12 months postoperatively
|
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AOFAS Ankle-Hindfoot Score
Time Frame: At least 12 months postoperatively
|
A validated 100-point scoring system for assessing ankle and hindfoot function.
Comprises three domains: pain (40 points), function (50 points), and alignment (10 points).
Higher scores indicate better function.
Score categories: Excellent 90-100; Good 80-89; Fair 65-79; Poor <65.
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At least 12 months postoperatively
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Böhler's Angle
Time Frame: Preoperative, immediate postoperative, and at least 12 months postoperatively
|
Change in Böhler's angle measured on lateral X-rays.
Böhler's angle is formed by the intersection of a line from the highest point of the anterior process to the highest point of the posterior facet and a line from the highest point of the posterior facet to the superior margin of the calcaneal tuberosity.
Normal range is approximately 20°-40°.
A decrease indicates loss of calcaneal height and posterior facet collapse.
|
Preoperative, immediate postoperative, and at least 12 months postoperatively
|
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Change in Gissane's Angle
Time Frame: Preoperative, immediate postoperative, and at least 12 months postoperatively
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Change in Gissane's angle measured on lateral X-rays.
Gissane's angle is formed at the intersection of the downward and upward slopes of the calcaneal superior surface, located beneath the lateral process of the talus.
Normal range is approximately 120°-140°.
An increase indicates architectural disruption of the posterior facet.
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Preoperative, immediate postoperative, and at least 12 months postoperatively
|
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Change in Calcaneal Height
Time Frame: Preoperative, immediate postoperative, and at least 12 months postoperatively
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Change in calcaneal height measured on lateral X-rays from preoperative to postoperative and final follow-up.
A decrease in calcaneal height indicates collapse of the fractured calcaneus.
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Preoperative, immediate postoperative, and at least 12 months postoperatively
|
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Change in Calcaneal Width
Time Frame: Preoperative, immediate postoperative, and at least 12 months postoperatively
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Change in calcaneal width measured on axial X-rays from preoperative to postoperative and final follow-up.
An increase in calcaneal width indicates lateral wall bulging after fracture.
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Preoperative, immediate postoperative, and at least 12 months postoperatively
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Postoperative Complications
Time Frame: Up to 12 months postoperatively
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Number of participants with postoperative complications, including wound infection, screw loosening, sural nerve injury, and other surgery-related adverse events.
Complications will be recorded during routine clinical follow-up.
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Up to 12 months postoperatively
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- PekingUTH ZF SUS Screw
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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