ClinicalTrials.gg
RecruitingNCT07773402TPFUpdated Aug 19, 2026

Comparison of Functional Outcome Between Locking Plate Technique Versus Hybrid Ilizarov Technique in Patients With Schatzker Type V and VI Tibial Plateau Fractures

An interventional study of Hybrid Ilizarov Fixation and Locking Plate Fixation in Tibial Plateau Fracture, sponsored by Prof. Sajjad Hussain Goraya. Recruiting at 1 site in Pakistan. Open to participants aged 25 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-08-19.

Sponsored by Prof. Sajjad Hussain Goraya · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
78
Allocation
Randomized
Ages
25 Years to 50 Years
Sex
All
01

Study summary

This comparative clinical study will evaluate and compare the functional outcomes of patients with Schatzker type V and VI tibial plateau fractures treated using either the locking plate technique or the hybrid Ilizarov technique. Functional outcome will primarily be assessed using the Rasmussen Knee Functional Score. Fracture healing, time to union, non-union, delayed union, and infection will also be assessed and compared between the two treatment groups.

Read the detailed description

Complex tibial plateau fractures, particularly Schatzker type V and VI fractures, are associated with substantial articular and metaphyseal injury and may present challenges in achieving satisfactory fracture reduction, stable fixation, soft-tissue preservation, and functional recovery.

The present comparative study will be conducted in the Orthopedic Department of Jinnah Hospital, Lahore. A total of 78 patients meeting the eligibility criteria will be recruited. Participants will be assigned to one of two treatment groups: Group A will undergo fixation using the hybrid Ilizarov technique, while Group B will undergo fixation using a locking plate technique.

Patients will undergo clinical and radiological assessment during follow-up. Functional outcome will be assessed using the Rasmussen Knee Functional Score. Radiographs will be obtained at regular follow-up intervals to evaluate fracture healing and union. Postoperative complications, including infection and non-union, will be documented.

The study will compare functional outcomes and fracture-healing outcomes between the two treatment techniques.

02

Conditions studied

  • Tibial Plateau Fracture

Keywords

  • Tibial plateau fracture
  • Schatzker type V
  • Schatzker type VI
03

In context

Tibial Plateau Fractures

32 studies on the registry are indexed under Tibial Plateau Fractures; 12 are open to participants now.

This study's planned enrollment of 78 is above the median of 56 across 21 interventional studies indexed under Tibial Plateau Fractures.

Browse Tibial Plateau Fractures studies →

Lead sponsor

This is the only study on the registry with Prof. Sajjad Hussain Goraya as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients of either sex.
  • Age between 25 and 50 years.
  • Patients presenting within 2 weeks of sustaining the fracture.
  • Patients diagnosed with complex tibial plateau fractures classified as Schatzker type V or VI.
  • Patients willing to participate in the study.
  • Patients providing written .

Exclusion criteria

Exclusion Criteria:

  • Associated ipsilateral limb fractures.
  • Pathological fracture of the tibia.
  • Associated major organ injuries.
  • Psychiatric illness that may interfere with participation or outcome assessment.
  • Refusal to provide .
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
78 participants (estimated)

Study arms

  • Experimental
    Hybrid Ilizarov Technique

    Patients with Schatzker type V or VI tibial plateau fractures will undergo fracture reduction and fixation using a hybrid Ilizarov external fixation technique. Closed or minimally open reduction will be performed under C-arm fluoroscopic guidance, followed by application of a hybrid Ilizarov frame using tensioned Kirschner wires and Schanz screws. Bone graft or bone substitute may be used when clinically indicated.

    Procedure: Hybrid Ilizarov Fixation

  • Active comparator
    Locking Plate Technique

    Patients with Schatzker type V or VI tibial plateau fractures will undergo fracture reduction and internal fixation using a locking compression plate under C-arm fluoroscopic guidance. Appropriate medial and/or lateral plate fixation will be performed according to fracture configuration and stability. Bone grafting may be used when clinically indicated.

    Procedure: Locking Plate Fixation

Interventions

  • ProcedureHybrid Ilizarov Fixation

    Patients with Schatzker type V or VI tibial plateau fractures will undergo fracture reduction and fixation using a hybrid Ilizarov external fixation system under C-arm fluoroscopic guidance. Closed or minimally open reduction will be performed as appropriate. The construct will consist of a hybrid Ilizarov C-ring with appropriately tensioned Kirschner wires and Schanz screws. Additional wires or fixation components may be used when required to achieve adequate fracture stability and alignment. Bone graft or bone substitute may be used when clinically indicated.

  • ProcedureLocking Plate Fixation

    Patients with Schatzker type V or VI tibial plateau fractures will undergo fracture reduction and internal fixation using a locking compression plate under C-arm fluoroscopic guidance. The appropriate surgical approach and medial and/or lateral plate configuration will be selected according to fracture morphology, comminution, and stability. Bone graft or bone substitute may be used when clinically indicated. Postoperative rehabilitation will include early knee range-of-motion exercises, non-weight-bearing ambulation initially, and progressive weight-bearing according to clinical and radiological fracture healing.

06

What researchers measure

Primary outcomes

  1. Rasmussen Knee Functional Score

    Functional outcome will be assessed using the Rasmussen Knee Functional Score at the final postoperative assessment. Scores will be categorized as excellent (27-30), good (20-26), fair (10-19), or poor (6-9). The score will be compared between patients treated with hybrid Ilizarov fixation and those treated with locking plate fixation.

    Time frame: 8 weeks and 16 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Aug 2026; primary completion for Nov 2026, 3 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 15, 2026
First posted
Aug 19, 2026
StartEst.
Aug 16, 2026
Primary completionEst.
Nov 16, 2026
CompletionEst.
Nov 16, 2026
Last update
Aug 19, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07773402
Lead sponsor
Prof. Sajjad Hussain Goraya
Responsible party
Prof. Sajjad Hussain Goraya (Principal Investigator, Allama Iqbal Medical College) — Sponsor-investigator
First posted
Aug 19, 2026
Start date
Aug 16, 2026 (estimated)
Primary completion
Nov 16, 2026 (estimated)
Completion
Nov 16, 2026 (estimated)
Last update
Aug 19, 2026

Study contacts

Sajjad Hussain
Contact
prof.sajjadhussain@aimc.edu.pk
0333 4077389
Montiha Azeem
Contact
muntahaazeem9@gmail.com
03479717317

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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