Actively Recruiting

Age: 18Years - 55Years
All Genders
ID07248982

Prospective Cohort Study of High-Strength Suture Modified Tension Band Technique for the Treatment of Patellar Fractures

Led by Fuzhou University Affiliated Provincial Hospital · Updated on 2025-11-25

50

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the clinical effectiveness of a high-strength suture modified tension band fixation in treating patellar fractures compared to the traditional screw-cable tension band fixation. This prospective cohort study focuses on adult patients aged 18 to 55 years with specific types of patellar fractures (AO/OTA 34-C1 or 34-C2). The study aims to assess knee function, pain, and motion after surgery, as well as secondary outcomes like healing time, complications, and patient satisfaction over a 12-month follow-up period. Patients admitted for patellar fracture surgery will be assigned to one of two groups based on the surgical method used: the high-strength suture fixation group or the traditional screw-cable tension band group. Both procedures involve surgery to repair the fracture, with the study comparing outcomes such as surgical time, blood loss, hospital stay, and complication rates. Follow-up visits include clinical assessments and imaging to monitor healing and alignment. Participants will undergo evaluations including knee function scores, range of motion measurements, pain scales, muscle strength testing, and patient satisfaction surveys at multiple timepoints up to 12 months after surgery. Data collected covers demographics, fracture details, comorbidities, and perioperative information. Adverse events will be recorded and managed. The research team will analyze the data to compare the two fixation methods and publish the results.

CONDITIONS

Brief Title

High-Strength Suture vs. Traditional Tension Band for Patellar Fractures

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 55 years
  • Radiographically confirmed patellar fracture (AO/OTA 34-C1 or 34-C2)
  • First-time patellar fracture surgery
  • Time from injury to surgery 2 weeks or less
  • Able to comply with follow-up and provide written informed consent
  • Normal knee function before injury
  • Able to tolerate surgery and agree to surgical treatment
  • Intact cognitive function
Not Eligible

You will not qualify if you...

  • Age younger than 18 or older than 55 years
  • Pathological fractures
  • Prior patellar surgery or severe underlying patellofemoral disease
  • Time from injury to surgery more than 2 weeks
  • Active infection or severe medical conditions
  • Severe neuropsychiatric disorders affecting follow-up
  • Postmenopausal women
  • Unable to tolerate surgery or refusal of surgery
  • Comorbid patellar dysplasia, rheumatoid arthritis, or other patellofemoral diseases
  • Systemic or local infection at surgical site
  • Severe lower limb or systemic injuries
  • Pre-injury cognitive impairment, mental disorder, or independent walking disability
  • Other conditions unsuitable for enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Day of surgery

Participants undergo surgery for patellar fracture using either high-strength suture modified tension band fixation or traditional screw-cable tension band fixation.

1 visit (in-person)

Post-operative Follow-up

Duration - 12 months

Participants are followed up to assess healing, knee function, pain levels, muscle strength, and any complications after surgery.

Visits at approximately 1 week, 6 weeks, 1 month, 3 months, 6 months, and 12 months postoperatively

Trial Site Locations

Total: 1 location

1

Fuzhou University Affiliated Provincial Hospital

Fuzhou, Fujian, China, 350001

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Research Team

A

Anning Liu, M.Med. (candidate)

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Suture tension band fixation vs. metallic tension band wiring for patella fractures - A biomechanical study on 19 human cadaveric patellae.

Jonas Adjal, Asger Haugaard, Liv Vesterby...

https://pubmed.ncbi.nlm.nih.gov/35701245

A new and effective tension-band braided polyester suture technique for transverse patellar fracture fixation.

Seán C A Hughes, Philip M Stott, Anthony J Hearnden...

https://pubmed.ncbi.nlm.nih.gov/17098238

Nonmetallic tension band fixation is a viable and low-complication surgical technique in patellar fractures: a five-year retrospective study.

Rovere Giuseppe, Romeo Michele, Farinelli Luca...

https://pubmed.ncbi.nlm.nih.gov/38530504

Tension band high-strength suture combined with absorbable cannulated screws for treating transverse patellar fractures: finite element analysis and clinical study.

Feifan Xiang, Yukun Xiao, Dige Li...

https://pubmed.ncbi.nlm.nih.gov/38515618