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The Effect of Percutaneous Kirschner Wire Technique in Management of CPT Under One Year Old

H

Hunan Children's Hospital

Status

Unknown

Conditions

Congenital Pseudarthrosis of Tibia

Treatments

Device: kirschner wire

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study was to investigate the effect of percutaneous kirschner wire in management of Congenital Pseudarthrosis of Tibia in children younger than 1 year of age. This study was to determine the union rates of congenital pseudarthrosis in children operated before 1 year of age to identify growth abnormalities in the affected limb ,including ankle valgus,tibia valgus,and shortening.

Full description

Currently, the timing of surgery for congenital pseudarthrosis of the tibia is a controversial issue. The investigators use percutaneous kirschner wire technique to manage the Congenital Pseudarthrosis of Tibia in children younger than 1 year of age.To investigate the effect of percutaneous kirschner wire in management of Congenital Pseudarthrosis of Tibia in children younger than 1 year of age. Bone uion rate,average time of healing, ankle valgus, limb length discrepancy, tibia axis alignment are recorded and evaluated.

Enrollment

100 estimated patients

Sex

All

Ages

1 to 12 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients did not undergo procedures
  • Patients with Crawford type IV CPT treated with Percutaneous Kirschner wire techniques
  • The age during surgery was less than 12 months old

Exclusion criteria

  • Patients with pseudarthrosis of tibia caused by trauma,infection, etc

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

surgery
Experimental group
Description:
Percutaneous Kirschner wire
Treatment:
Device: kirschner wire

Trial contacts and locations

1

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Central trial contact

Haibo Mei, MD; Kun Liu, MD

Data sourced from clinicaltrials.gov

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