Comparative Study of Gene-activated Bone Substitute and Autobone in Treatment of Long Bone Nonunions

Histograft Co., Ltd.20 enrolled

Overview

The study is aimed to compare the effectiveness of "Histograft" bone substitute (gene-activated bone substitute based on octacalcium phosphate and plasmid DNA encoding VEGFA gene) mixed with shredded autobone and pure shredded auto bone harvested from iliac crest in treatment of patients with long bone nonunions

An open-label randomized controlled clinical trial, two cohorts. Patients who met the inclusion criteria are planned to be enrolled into the trial. Upon enrollment, all patients will undergo screening, a set of clinical examination, instrumental investigations and laboratory tests, including CT of the affected bone with the assessment of nonunion. All patients enrolled in the study will be subjected to bone reconstructive surgery with nonunion excision and bone grafting with either investigational bone substitute mixed with shredded autobone (in a ratio of 50/50) harvested during the surgery or pure shredded autobone from iliac crest. The clinical study results will be evaluated at the time points of 1, 15, 45, 90, 180 days with clinical examination, instrumental investigations and laboratory tests. Control CT will be carried out for the primary outcome measure at 90, 180, 360 days after surgery.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Non Union Fracture Non-Union of Ankle Joint Without Infection

Interventions

"Histograft", a bone substitute based on octacalcium phosphate (OCP) and plasmid DNA encoding VEGFA geneCOMBINATION_PRODUCT

gene-activated bone substitute in granular form, concentration of the plasmid DNA is 100 μg per 1.0 g of the OCP scaffold

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * traumatic isolated closed or open Gustilo I and II, IIIA and IIIB humerus, tibial or femur diaphyseal or metaphysodiaphyseal fracture with a status of atrophic, oligotrophic or normotrophic non-union; * signed voluntary informed consent Exclusion Criteria: * hypertrophic non-union; * disability or unwillingness to give a voluntary informed consent or follow requirements of the clinical trial; * segmental bone loss requiring specific therapy (bone transport, vascularized graft, large structural allograft, megaprosthesis, etc); * other fractures causing interference with weight bearing; * visceral injuries or diseases interfering with callus formation (severe cranioencephalic trauma, etc.); * unrecovered vascular or neural injury; * infection of any location and aetiology; * pregnancy, breast feeding women and women who are of childbearing age and not practicing adequate birth control; * malignant tumour (past history or concurrent disease); * history of bone harvesting on iliac crest contraindicating new iliac crest bone graft harvesting or bone marrow collection; * conditions limiting study compliance (e.g., dementia, psycho-neurological diseases, drug addiction, and alcoholism); * medication affecting bone turnover (oral bisphosphonates, PTH, sodium fluoride, strontium ranelate, calcitonin, testosterone, systemic cortico- or anabolic steroids)

Locations (1)

S.M. Kirov Military Medical Academy, Department of Traumatology and Orthopaedics

Saint Petersburg, Russia

Outcomes

Primary Outcomes

Bone consolidation

Radiographic assessment of bone healing using REBORNE scale

Time frame: 12 months

Secondary Outcomes

Adverse Events and Serious Adverse Events

Evaluation of the Adverse Events and Serious Adverse Events frequency

Time frame: 12 months

Ability to use the operated limb

Clinical assessment using DASH scale (for upper limb) or LEFS scale (for lower limb)

Time frame: 12 months

Pain level

Level of pain measured using Numeric Rating Scale

Time frame: 12 months

Data from ClinicalTrials.gov

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