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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01328418
Other study ID # Akondroplazi - Bilen
Secondary ID
Status Completed
Phase N/A
First received April 1, 2011
Last updated April 1, 2011
Start date April 2002
Est. completion date March 2011

Study information

Verified date April 2011
Source Bilen, Fikri Erkal, M.D.
Contact n/a
Is FDA regulated No
Health authority Turkey:Institute for Drugs and Medicine Devices
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether lengthening of both the tibiae and femora in achondroplastic patients is safe and provides reproducible outcome.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date March 2011
Est. primary completion date March 2008
Accepts healthy volunteers No
Gender Both
Age group 3 Years to 11 Years
Eligibility Inclusion Criteria:

- Achondroplasia, first lengthening period

Exclusion Criteria:

- Previous lengthening

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Lengthening over nail
External fixator is used to lengthen either the femur or the tibia over an intramedullary nail

Locations

Country Name City State
Turkey Istanbul Medical School Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Bilen, Fikri Erkal, M.D.

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Paley's functional scoring system Paley's functional scoring system evaluates the results after lengthening or deformity correction procedures: residual limb length discrepancy, any brace or other aid usage, joint contracture, pain, soft tissue dystrophism Minimum 2 year follow-up No