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Autologous BM-MSC Transplantation in Combination With Platelet Lysate (PL) for Nonunion Treatment

Use of Autologous Bone Marrow Derived Mesenchymal Stromal Cells in Combination With Platelet Lysate Product for Human Long Bone Nonunion Treatment, A Phase 2-3 Clinical Trial

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02448849
Enrollment
60
Registered
2015-05-20
Start date
2015-06-30
Completion date
2017-08-31
Last updated
2015-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Fracture

Keywords

Autologous, nonunion fracture, bone marrow, mesenchymal, stromal cell, platelet lysate product

Brief summary

Nonunion of long bones would occur in almost 10% of fractures and because of its long term and complicated treatment, is known as a therapeutic challenge for both of the surgeons and patients. Cell therapy is useful in treatment of nonunion and mesenchymal stromal/stem cells are the best candidates for this kind of treatment. Percutaneous implantation of autologous bone marrow derived mesenchymal stromal/stem cell in combination with PL will be done in 30 patients with tibia nonunion. The other 30 patients as the control group will receive placebo. The patients will be followed at 2weeks, 3months, 6m and 12 months after implantation. The Spss(v16) software will be used for data analysis.

Detailed description

Long bone nonunion is known as a therapeutic challenge for both the orthopedic surgeons and the society. Current treatment of this disorder is autologous bone graft. This treatment has potential minor and major complications and is considered as a risky treatment. So researches are focused on new treatment approaches for this disease. Cell therapy is one of these new approaches especially based on mesenchymal stromal cells. The investigators will evaluate safety and efficacy of percutaneous implantation of autologous BM-MSC (bone marrow -derived mesenchymal stromal cell) in combination with PL (platelet lysate product) in 30 tibia nonunion patients. The other 30 patients will receive placebo. These patients will be followed up and data will be analyzed with spss(v16).

Interventions

percutanous implantation of bone marrow derived mesenchymal stromal cells in patients with nonunion fracture.

Sponsors

Royan Institute
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Non-united fracture of tibial midshaft at X-ray. * Non-united gap less than 1cm. * Fracture has fixed by closed intramedullary rod. * Hypotrophic type. * At least 6 months after initial surgery. * Patient informed consent.

Exclusion criteria

* Infected nonunion * Multiple major fracture * Non treated major fracture * malignancy * Pregnancy or lactating * Uncontrolled chronic diseases, such as: diabetes mellitus, hypertension, renal diseases, liver diseases, thyroid diseases, heart diseases, blood diseases, etc. * Steroid usage. * Positive test for HIV and/or HBS and/or HBC and/or HTLV (1,2) * Fracture site more than 1 cm.

Design outcomes

Primary

MeasureTime frameDescription
clinical union3months\- Clinical union is defined as an asymptomatic patient who was able to fully bear weight on the injured leg
Radiological healing1week\- radiographic fracture healing is defined by bone continuity (bony bridging) present in three out of four cortices in two projections (anterior-posterior & lateral x-rays), assessed by a blinded senior orthopedic surgeon. CT scan, for confirm the results - radiolographic fracture healing is defined by bone continuity (bony bridging) present in three out of four cortices in two projections (anterior-posterior & lateral x-rays), assessed by a blinded senior orthopedic surgeon. CT scan, for confirm the results \- radiolographic fracture healing is defined by bone continuity (bony bridging) present in three out of four cortices in two projections (anterior-posterior & lateral x-rays), assessed by a blinded senior orthopedic surgeon. CT scan, for confirm the results

Secondary

MeasureTime frameDescription
Pain3monthsThe pain relief as measured by Visual Analogue Scale (VAS) 3 months after cell injection
Quality of life3monthsEvaluation the patients' quality of life with Visual Analogue Score (VAS) 3months after cell transplantation.
Walking distance3monthsWalking distance changes as measured by walking on treadmill 3 months after cell injection.

Countries

Iran

Contacts

Primary ContactNasser Aghdami, MD, PhD
nasser.aghdami@royaninstitute.org(+98)23562000
Backup ContactLeila Arab, MD
Leara91@gmail.com(+98)23562000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026