Percutaneous Autologous Bone-marrow Grafting for Open Tibial Shaft Fracture

Not Applicable

Completed

• Conditions: Fractures, Open; Tibial Fractures
• Interventions: Procedure: Osteosynthesis

• Registration Number: NCT00512434
• Lead Sponsor: University Hospital, Tours

Brief Summary

The treatment of open tibial shaft fracture is often complicated by delayed union or non-union. The objective of this study is to evaluate the efficacy of autologous concentrated bone-marrow to accelerate healing of open tibial shaft fractures and to reduce the need for secondary intervention.

In a prospective, randomized, controlled, single-blind study, 186 patients with an open tibial will be randomized to receive either the standard of care (fixation by nail or external fixator and routine soft-tissue management), or the standard of care with percutaneous injection, one month after fracture, of autologous concentrated bone-marrow. Randomization will be stratified by severity of the open wound. The primary outcome measure will be the proportion of patients requiring secondary intervention because of delayed union or nonunion within twelve months post-fracture.

Detailed Description

This study will be conducted at 13 University Hospitals in France. The protocol has been approved by the institutional review board. After written informed consent, patients will be randomized, in the days after the fracture in 2 groups of 93 patients : 1) the control group (standard of care only: fixation by nail or external fixator and routine soft-tissue management) and 2) the study group (standard of care with percutaneous injection, one month after fracture, of autologous concentrated bone-marrow). Randomization will be stratified by severity of the open wound and by center. For the wound, strata A comprise Gustilo-Anderson types I, II and III-A and strata B, type III-B.

For the study group, the injection is scheduled at 1 month ± 5 days after the fracture. The techniques have been described by Hernigou (J Bone Joint Surg Am, 2006; 88(sup 1 part 2): 322-327). There are 3 steps: marrow aspiration (300 - 500 g) from iliac crest under general anesthesia, centrifugation in cell therapy unit to obtain a concentrated buffy coat of about 50 ml containing progenitor cells and other mononuclear cells, percutaneous injection in the fracture site of 20-30 ml of the buffy coat under fluoroscopy control.

Apart from the injection, the standard of care is the same for the 2 groups. Patients will be followed for 12 months, with assessments at 1, 2, 3, 6, 9 and 12 months.

All analysis will be based on the intent to treat the population. The primary outcome measure will be the proportion of patients requiring secondary intervention because of delayed union or nonunion within twelve months post fracture. An independent panel of surgeons will evaluate all secondary procedure with the potential of promoting fracture-healing.

An independent evaluation of fracture union will be conducted by a radiology panel blinded to treatment allocation and all other patient data.

An outcome will be considered to be successful when the fracture heal, according to the investigator, without secondary intervention and is radiographically united during patient follow-up.

Study Timeline

• Study First Submitted: 2007-08-06
• Study First Submitted QC: 2007-08-06
• Study First Posted: 2007-08-07
• Study Start: 2007-09
• Primary Completion: 2012-09
• Study Completion: 2013-09
• Status Verified: 2018-10
• Last Update Submitted: 2018-10-19
• Last Update Posted: 2018-10-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 85

Inclusion Criteria

• Age 17 years or more
• Open tibial shaft fracture with Gustilo-Anderson type I, II, III A or B
• Written informed consent
• Affiliated to French Social Security

Exclusion Criteria

• Circumferential bone loss
• Vascular or nerve injury
• Injury, other than tibial fracture, interfering with weight bearing
• Infection (skin, soft-tissue or bone)
• Disease or treatment interfering with bone union: head injury with coma, pathologic fracture
• Medical history on iliac wing contraindicating bone-marrow aspiration
• Corticoid or immunosuppressive therapy more than one week
• Pregnancy at the day of inclusion in study
• History of positive serology for HIV1+2, HBs, HCV
• Adult in the care of a guardian
• Impossibility to meet at the appointments for the follow-up

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control in arm fields	Osteosynthesis	Standard treatment Intervention no'Osteosynthesis'
IMOCA	Osteosynthesis	Intervention 'Osteosynthesis' Percutaneous autologous bone-marrow grafting - surgical technique (ref: Hernigou Ph et al J Bone Joint Surg Am ,2006; 88 (sup 1 part 2): 322-327

Primary Outcome Measures

Name	Time	Method
Proportion of patients requiring secondary intervention because of delayed union or nonunion within twelve month post fracture.	one year

Secondary Outcome Measures

Name	Time	Method
Relation between the number of the progenitor available injected with concentrated bone marrow aspirated and the rate of bone union.	one year
Comparison of the rate of complications between the 2 groups.	one year
Economic impact study.	one year

Trial Locations

Locations (11)

UH Clermont Ferrand Gabriel Montpied; 🇫🇷 Clermont Ferrand, France

UH Grenoble Michallon Hospital; 🇫🇷 Grenoble, France

UH Pitié Salpétrière AH HP; 🇫🇷 Paris, France

UHTOURS; 🇫🇷 Tours, France

UH Angers; 🇫🇷 Angers, France

UH Grenoble South Hospital; 🇫🇷 Grenoble, France

UH Besançon Jean Minjoz; 🇫🇷 Besancon, France

UH Nancy Central Hospital; 🇫🇷 Nancy, France

UH Tours CHRU Trousseau; 🇫🇷 Tours, France

UH Brest Cavale Blanche; 🇫🇷 Brest, France

UH Nantes Hôtel Dieu; 🇫🇷 Nantes, France