Completed

Phase II Clinical Trial of Tissue Engineering Based on the Use of Mononuclear Cells From Autologous Bone Marrow Seeded on Porous Tricalcium Phosphate Biomaterial in Patients With Pseudoarthrosis

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What is being tested

ABM seeded onto a porous TCP and DBM

+ autologous bone graft

Procedure
Who is being recruted

Fractures, Ununited+1

+ Wounds and Injuries

+ Pseudarthrosis

From 18 to 75 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 2
Interventional
Study Start: April 2011
See protocol details

Summary

Principal SponsorFundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia
Last updated: March 30, 2017
Sourced from a government-validated database.Claim as a partner

Study start date: April 1, 2011

Actual date on which the first participant was enrolled.

An estimated 10% of closed fractures and between 35-45% in cases of open fractures, are at risk of developing a delay in the process of consolidation or a complete failure of it (pseudoarthrosis) depending on location , severity of trauma on bone, soft tissue and vascular structures Some of these cases are refractory to all treatment methods available today, requiring numerous interventions with the potential risk for recurrent infections that they carry. For this reason, its treatment remains a challenge for the orthopedic surgeon. Recent advances in knowledge of cellular and molecular biology related to the mechanism of bone repair and biomaterials science have been joined in a new discipline called tissue engineering, its implementation in clinical practice is being done so progressive. Cell therapy based on the use of adult stem cells (MSCs) derived from autologous bone marrow, introduces new applications for the repair of fractures including pseudoarthrosis and avascular bone necrosis. Its mechanism of action does not focus only on their local action, but also in the release of signaling molecules with autocrine and paracrine action through recruitment and activation of endogenous MSCs to osteoblastic differentiation and bone tissue regeneration. On the other hand, the seeding of MSCs on biomaterials (natural or synthetic) is more effective, to facilitate adherence, proliferation and extracellular matrix production in the area where implanted. Today, the investigators can say that there are experimental and clinical evidence supporting the effectiveness of the method. The investigators have designed a phase II clinical trial to check the feasibility of this approach.

Principal SponsorFundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia
Last updated: March 30, 2017
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

5 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 75 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Fractures, UnunitedWounds and InjuriesPseudarthrosisFractures, Bone

Criteria

Inclusion Criteria: Pseudarthrosis of tibia established any cause with at least 9 months. The pseudarthrosis is not to show signs of healing in the last 3 months. The pseudarthrosis subsidiary should not be solely osteosynthesis treatment. Age between 18 and 75 years. Serology Human Immunodeficiency virus (HIV), hepatitis B virus (HBV) and hepatitis C virus (HCV) negative. Negative pregnancy test in women of childbearing age. Patient sufficient guarantees of adherence to protocol. Signature written informed consent before a witness Exclusion Criteria: Systemic infection. Septic pseudoarthrosis. Insufficient skin coverage at the site of nonunion. Vascular insufficiency in the affected limb. Pathological fracture. Concomitant psychiatric or neurological disease. Concurrent or prior malignancy treated with chemotherapy over a period of less than 1 year. Concomitant severe disease not well controlled. Inclusion in other clinical trials. Inability to understand the informed consent

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
ABM seeded onto a porous TCP and DBM

Group II

Active Comparator
autologous bone graft

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Hospital UniversitarioVirgen de la Arrixaca

El Palmar, SpainOpen Hospital UniversitarioVirgen de la Arrixaca in Google Maps
CompletedOne Study Center