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NCT Number: NCT07831265

Dynamic Fixation for Complex Ankle Fractures With Syndesmotic Diastasis.

This prospective randomized controlled trial aims to evaluate the clinical effectiveness of dynamic fixation in patients with complex ankle fractures associated with syndesmotic diastasis.

Patients undergoing surgical treatment for complex ankle fractures with syndesmotic diastasis at Fujian Provincial Hospital Affiliated with Fuzhou University between October 2026 and October 2027 will be enrolled. Eligible participants will be randomly assigned in a 1:1 ratio to either the screw fixation (SF) group or the dynamic fixation (DF) group. All participants will be followed for 12 months after surgery. Clinical, functional, and radiographic outcomes will be compared between the two groups to assess the effectiveness and safety of dynamic fixation.

Statistical analyses will be performed using IBM SPSS Statistics version 27.0. The primary analysis will follow the intention-to-treat principle. Appropriate statistical methods will be selected according to the type and distribution of the data. Multivariable regression analyses will be performed when necessary to adjust for potential confounding factors. Missing data will be handled using multiple imputation where appropriate, and sensitivity analyses will be conducted to evaluate the robustness of the findings. All statistical tests will be two-sided, with a P<0.05 considered statistically significant.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-55 years
  • Radiologically confirmed complex ankle fracture combined with distal tibiofibular syndesmosis separation
  • First-time surgical treatment of the ankle
  • Time from injury to surgery ≤ 2 weeks
  • Able to comply with follow-up and sign a written informed consent
  • Ankle function was basically normal before injury

Exclusion criteria

  • Age <18 or >55
  • Pathological fracture
  • Previous ankle surgery or serious primary ankle disease
  • Time from injury to surgery >2 weeks
  • Active infection or serious medical condition
  • Severe neurological or psychiatric disorder affecting follow-up compliance
  • Postmenopausal women
  • Other situations not suitable for enrollment

Treatment and study plan

the dynamic fixation

Device

Randomized controlled grouping was conducted under blind conditions, followed by treatment of complex ankle fractures with distal tibiofibular syndesmosis separation using dynamic internal fixation surgical methods.

the screw fixation

Device

"Randomized controlled grouping was conducted under blind conditions, followed by treatment of complex ankle fractures with distal tibiofibular syndesmosis separation using screw fixation surgical methods.

Primary outcomes

  1. The American Orthopaedic Foot and Ankle Society (AOFAS)

    Time frame: Preoperative; 1 week, 1 month, 3 months, 6 months, 1 year postoperative

    The American Orthopaedic Foot and Ankle Society (AOFAS) , Ankle-Hindfoot Score ranges from a minimum of 0 to a maximum of 100, with higher scores indicating better ankle-hindfoot function and fewer symptoms.

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Sponsors and collaborators

Lead sponsor

Fuzhou University Affiliated Provincial Hospital

Other

Registry information

Official study title

A Prospective Randomized Controlled Trial of Dynamic Fixation for Complex Ankle Fractures With Syndesmotic Diastasis.

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Sep 21, 2026
Registry last updated
Sep 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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