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Observational Retrospective Study on the Clinical and Radiographic Outcomes of the Aseptic Pseudarthrosis Treatment of the Upper Limb

I

Istituto Ortopedico Rizzoli

Status

Completed

Conditions

Pseudarthrosis

Treatments

Other: biological adjuvants
Other: no biological adjuvants

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to collect boh clinical and radiographic data coming from the treated patients for pseudarthrosis of the upper limbs from 2000 to 2017 at the SC Orthopedic Surgery, Innovative Techniques of the Istituto Ortopedico Rizzoli in order to evaluate the clinical and radiographic outcomes of the treatment, with or without the application of biological adjuvants.

Full description

The bone healing requires the integrations of two main principles: biomechanical aspect and biological aspect. The second one has having growing interest.

The use of the biological adjuvants, as growth factors (rhBMP2 and 7), platelet-derived growth factors (PDGFs), Platelet gel (PG) or Plasma Rich Fibrin (PRF), as well as peptides and molecules are demonstrating promising results in the field of bone regeneration.

The addition of autologous bone marrow concentrate cells has proven to be an effective option in the treatment of bone defects, although to date there is no clear superiority of one method over the other.

In light of this, the purpose of the study is to evaluate the clinical and radiographic outcomes of the treatment, with or without the application of biological adjuvants, collecting data coming from the treated patients for pseudarthrosis of the upper limbs from 2000 to 2017 at the SC Orthopedic Surgery, Innovative Techniques of the Istituto Ortopedico Rizzoli

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with post-traumatic pseudoarthrosis of the long bones of the upper limb
  • Duration of at least 6-9 months without clinical-radiographic signs of healing in the 3 months prior to pseudoarthroses

Exclusion criteria

  • Pseudoarthrosis due to pathological fracture
  • Infected pseudarthrosis
  • Pseudoarthrosis treated with external fixation
  • BMI> 35

Trial design

90 participants in 2 patient groups

biological adjuvants
Description:
patients with aseptic pseudarthrosis clinically treated with biological adjuvants
Treatment:
Other: biological adjuvants
without biological adjuvants
Description:
patients with aseptic pseudarthrosis clinically treated without biological adjuvants
Treatment:
Other: no biological adjuvants

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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