ClinicalTrials.Veeva

Menu

Human Bone Graft in Epiphysiodesis

Medical University of Vienna logo

Medical University of Vienna

Status

Enrolling

Conditions

Primordial Gigantism
Leg Length Differences

Treatments

Procedure: epiphysiodesis

Study type

Observational

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

This observational study is to document the application of human bone graft in the surgical treatment (epiphysiodesis) of leg length discrepancy or primordial gigantism and its subsequent healing process.

Enrollment

20 estimated patients

Sex

All

Ages

10 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Planned epiphysiodesis to stop the growing of a bone indicated by leg length discrepancies or primordial gigantism
  • Age 10-18 years
  • Written consent to participate in the study after previous written and oral education (additional consent for the participation of minors in the study after prior written and oral education by at least one parent)

Exclusion criteria

  • Insufficient knowledge of the german language
  • Foreseeable compliance issues
  • Neoplastic diseases, malignant bone tumors, rheumatoid arthritis
  • Patients with non-treated pre-existing conditions, which could be the cause of leg length differences
  • Active osteomyelitis
  • Ulcerations in the area of the skin of the surgical area
  • Immunosuppressive drugs that can not be discontinued

Trial design

20 participants in 1 patient group

human bone graft screw
Description:
human bone graft screws will be used during the epiphysiodesis
Treatment:
Procedure: epiphysiodesis

Trial contacts and locations

1

Loading...

Central trial contact

Sandra Hacker, MSc; Catharina Chiari, Dr.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems