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Clinical Trials/NCT03129230
NCT03129230
Completed
Not Applicable

Yulin Orthopedics Hospital of Chinese and Western Medicine

Yulin Orthopedics Hospital of Chinese and Western Medicine2 sites in 1 country16 target enrollmentAugust 1, 2012
ConditionsBone Diseases

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone Diseases
Sponsor
Yulin Orthopedics Hospital of Chinese and Western Medicine
Enrollment
16
Locations
2
Primary Endpoint
change of peri-implant bone level from baseline at 7 and 54 months
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study was to evaluate the safety and efficacy of free nonvascularized fibula autograft in the treatment of the femoral neck tumor-like lesions before epiphyseal closure in pediatric patients, by presenting the clinic-radiological outcome and complications.

Registry
clinicaltrials.gov
Start Date
August 1, 2012
End Date
March 1, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Yulin Orthopedics Hospital of Chinese and Western Medicine
Responsible Party
Principal Investigator
Principal Investigator

Shanchao Luo

Director

Yulin Orthopedics Hospital of Chinese and Western Medicine

Eligibility Criteria

Inclusion Criteria

  • This retrospective study included pediatric patients before epiphyseal closure with tumor-like lesions in femoral neck.

Exclusion Criteria

  • pediatric patients with tumor-like lesions in femoral neck after epiphyseal closure;
  • pediatric patients with benign bone tumors and malignant bone tumors in the femoral neck after epiphyseal closure;
  • adult patients with benign or malignant bone tumors and tumor-like lesions in femoral neck.

Outcomes

Primary Outcomes

change of peri-implant bone level from baseline at 7 and 54 months

Time Frame: 7 months to 54 months

Mean follow-up of all the patients after primary surgery was 24 months, ranged 7 months to 54 months.

Study Sites (2)

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