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Not yet recruiting NCT07505433

Ultrasound Monitoring of Bone Healing in Ilizarov Bone Transport

— Observational Bone Healing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ultrasound.
Who it may be relevant to
Registry conditions: Bone Healing. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Role of Ultrasound in Assessment of the Bony Union in Bone Transport by Ilizarov Frame

Overview

This prospective study evaluates the role of ultrasound in assessing bony union during Ilizarov bone transport. Ultrasound findings will be compared with radiographic and clinical outcomes to determine its accuracy in detecting early bone healing and predicting mechanical stability. The study aims to establish ultrasound as a reliable, radiation-free tool to guide safe frame dynamization and removal.

Interventions

  • Device Ultrasound
    Patients with bone defect undergoing bone transport by Ilizarov frame

Primary outcome measures

  • The role of Ultrasound in assessment of the bony union in bone transport by Ilizarov frame [Time frame: Baseline]
Secondary outcome measures (1)
  • The role of Ultrasound in assessment of the bony union in bone transport by Ilizarov frame [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Patients who will have Ilizarov bone transport,bone lengthening or corrective osteotomy

Exclusion criteria

  • Otherwise bone transport,bone lengthening or corrective osteotomy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07505433 · RUS-ABU-BT-IF

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗