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CompletedNCT04958564Updated Jul 12, 2021

Comparison of Interlock Nailing Versus Dynamic Compression Plating in Transverse Fractures of Tibia

An interventional study of DCP in Transverse Fracture of Shaft of Tibia, sponsored by District Headquarters Teaching Hospital Sahiwal. Completed at 1 site in Pakistan. Per ClinicalTrials.gov, last updated 2021-07-12.

Sponsored by District Headquarters Teaching Hospital Sahiwal · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 2 years 5 months after the study started (first participant enrolled Jan 2019, registered Jun 2021).
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Sex
All
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Study summary

Study aims to compare two treatment modalities for treatment of transverse fractures of tibia. One is Intramedullary interlocking nail and the other is dynamic compression plate.

Read the detailed description

This study is a comparison of two devices used to teat transverse fractures of tibia and these include intra medullary rod popularly known as intra medullary nail and the second is a weight bearing device know as dynamic compression plate which is fixed with screws to diaphyseal segment of bone.

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Conditions studied

  • Transverse Fracture of Shaft of Tibia
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In context

Lead sponsor

District Headquarters Teaching Hospital Sahiwal is the lead sponsor of 4 studies on the registry; none are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

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 with closed transverse tibial fractures

Exclusion criteria

Exclusion Criteria:

  • Patients unsuitable for surgical intervention
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
70 participants (actual)

Study arms

  • Active comparator
    group interlock

    Intra medullary device used to treat tibial shaft fractures

    Device: DCP

  • Active comparator
    group DCP (dynamic compression plate)

    dynamic compression plate used to treat tibial shaft fractures

    Device: DCP

Interventions

  • DeviceDCP

    1. Dynamic compression plating to compress the fracture 2. Intramedullary device to share the load.

    Also known as: Interlock nailing

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What researchers measure

Primary outcomes

  1. weight bearing

    when patient started to fully bear weight on affected leg after intervention

    Time frame: 12 weeks

Secondary outcomes

  1. time of union

    time for union during which three cortices of the bone seem united radiologically

    Time frame: 12 weeks

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Study locations

1 site
  • Orthopaedics Department ,DHQ Teaching Hospital Hospital Sahiwal
    Sahiwal, Punjab 57000, Pakistan
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References and documents

Individual participant data

Plan to share: Undecided — All data will probably be shared to fellow researchers after publication of study .

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04958564
Lead sponsor
District Headquarters Teaching Hospital Sahiwal
Responsible party
Humayun Israr (clinical professsor and dean of orthopaedics department, District Headquarters Teaching Hospital Sahiwal) — Principal investigator
First posted
Jul 12, 2021
Start date
Jan 20, 2019
Primary completion
Jan 20, 2020
Completion
Jan 20, 2020
Last update
Jul 12, 2021

Study contacts

Humayun Israr, MBBS
principal investigator · District Headquarters Teaching Hospital Sahiwal

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2021. You cannot join it, but the record below documents what was studied.

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