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Establishing registry of congenital pseudoarthrosis of tibia

Establishing a multi-centre congenital pseudarthrosis of the tibia treatment registry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012852
Enrollment
100
Registered
2018-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Congenital Pseudoarthrosis of tibia

Interventions

None listed

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Any child with a Crawford Type I, II, III or IV CPT who has not been treated prior to inclusion in the registry 2. Any child with Crawford Type I, II, III or IV CPT who has had a prior treatment that was unsuccessful in obtaining union (provided the details of the nature of treatment and all relevant radiographs are available for inclusion in the database of the registry)

Exclusion criteria

Exclusion criteria: Children with CPT who have had prior treatment and the details of the previous treatment are not available. Children with anterolateral bowing of the tibia due to other causes than CPT (which can be confused with Crawford Type I CPT)

Design outcomes

Primary

MeasureTime frame
Primary union, re-fracture, union at skeletal maturity, limb length discrepancy, limb deformityTimepoint: 3 months, 6 months, 1 year, 2 year, 3 year , 5 year, 7 year, 10 year, 13 years, Skeletal maturity limb deformity

Secondary

MeasureTime frame
Ankle valgus, tibia procurvatum, tibia varaTimepoint: 3 months, 6 months, 1 year, 2 year, 3 year , 5 year, 7 year, 10 year, 13 years, Skeletal maturity

Countries

Canada, India

Contacts

Public ContactDr Hitesh Shah

Kasturba Medical College, Manipal

hiteshshah12@gmail.com08202922755

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026