Tibial Delayed Healing Pivotal Clinical Trial
7 de enero de 2015 actualizado por: Medtronic Spinal and Biologics
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Evaluate the INFUSE/MASTERGRAFT™ Delayed Healing Device as an alternative/replacement to autograft in the treatment of tibial delayed healing.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
The purpose of this study is to evaluate the INFUSE/MASTERGRAFT™ Delayed Healing Device as an alternative/replacement to autograft in the treatment of tibial delayed healing.
A subject will be considered to have tibial delayed healing when he/she is at least six months from the date of the most recent surgical intervention and has shown no signs of radiographic healing for at least three months.
Radiographic signs of healing for this study are defined as either the progressive disappearance of fracture lines or the development of cortical continuity [bridging bone] at the site.
All prospective patients must require surgical treatment with rigid internal fixation [reamed IM nail or plate/screws] and bone grafting.
Tipo de estudio
Intervencionista
Inscripción (Actual)
23
Fase
- Fase 3
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Colorado
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Denver, Colorado, Estados Unidos, 80204
- Denver Health
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Florida
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Ft. Lauderdale, Florida, Estados Unidos, 33316
- Shrock Orthopedic Research
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Jacksonville, Florida, Estados Unidos, 32209
- University of Florida College of Medicine
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Orlando, Florida, Estados Unidos, 32806
- Orlando Health
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Indiana
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Fort Wayne, Indiana, Estados Unidos, 46804
- Fort Wayne Orthopaedics
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Indianapolis, Indiana, Estados Unidos, 46202
- Methodist Hospital
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Maryland
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Baltimore, Maryland, Estados Unidos, 21215
- Sinai Hospital of Baltimore
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Michigan
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Royal Oak, Michigan, Estados Unidos, 48073
- William Beaumont Hospital
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Missouri
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Columbia, Missouri, Estados Unidos, 65201
- University of Missouri
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St. Louis, Missouri, Estados Unidos, 63104
- St. Louis University Hospital
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New York
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Brooklyn, New York, Estados Unidos, 11220
- Lutheran Medical Center
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North Carolina
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Charlotte, North Carolina, Estados Unidos, 28204
- Carolinas Medical Center
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Ohio
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Columbus, Ohio, Estados Unidos, 43215
- Ohio Health Research Center
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Oklahoma
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Oklahoma City, Oklahoma, Estados Unidos, 73104
- University of Oklahoma
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Pennsylvania
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Danville, Pennsylvania, Estados Unidos, 17822
- Geisinger Clinic
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Tennessee
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Nashville, Tennessee, Estados Unidos, 37232
- Vanderbilt University Medical Center
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
21 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Has tibial delayed healing. A subject will be considered to have delayed healing when he/she is at least six months from the date of the most recent surgical intervention and has shown no signs of radiographic healing for at least three months. (Radiographic signs of healing for this study are defined as either the progressive disappearance of fracture lines or the development of cortical continuity [bridging bone] at the site.)
- Has delayed healing of the tibia that requires treatment with rigid internal fixation and bone grafting. (Stable rigid internal fixation hardware may already be in place prior to treatment. If required, the fixation hardware may be removed and replaced along with the placement of the bone graft.)
- Has adequate soft tissue coverage at the delayed healing site. All prior soft tissue coverage procedures (e.g., skin grafts or flaps) should be sufficiently healed for placement of a bone graft prior to enrollment in the study.
- Has a sufficient amount of iliac crest autograft available for a bone grafting procedure.
- After walking 5 or 6 steps, has intensity of pain/discomfort at the injury site equal to or greater than 4 (as reported on the preoperative Delayed Healing Site Pain Questionnaire form; 0 being no pain and 10 being pain as bad as it could be).
- Is at least 21 years of age and skeletally mature at the time of surgery.
- If a female of child-bearing potential, patient is not pregnant or nursing and agrees not to become pregnant for one year following surgery in the study.
- Is willing and able to comply with the study plan and able to understand and sign the Patient Informed Consent Form.
Exclusion Criteria:
- Has a congenital pseudarthrosis or pathological fracture nonunion (not including osteoporosis-related fractures).
- Has a tibial delayed healing with articular involvement (e.g., intra-articular). (The original fracture may have involved the joint, but the resulting delayed healing site may not involve the joint.)
- Has hypertrophic tibial delayed healing (e.g., observed on x-ray as having an abundant callus or "horse hoof" appearance).
- Has inadequate neurovascular status in the involved limb that may jeopardize healing.
- Has an active or a known prior infection at the delayed healing site (e.g., the presence of purulent drainage from the site, prior positive cultures from the site, or evidence of active/prior osteomyelitis at the site). Enrolled subjects whose intra-operative cultures test positive for bacteria may remain in the study.
- Has existing stable hardware that will not be removed and does not meet the algorithm requirements.
- Has treatment planned for the delayed healing that does NOT include placement of a bone graft and/or rigid internal fixation consisting of a reamed intramedullary nail or plate/screws.
- Has a tibial delayed healing injury site with a bony defect larger than 4 cm in length.
- Has another injury/condition that prevents ambulation or completion of any of the study assessments.
- Has a history of endocrine or metabolic disorder known to affect osteogenesis (e.g., Paget's disease, renal osteodystrophy, hyperthyroidism, parathyroid hormone disorder, Ehler-Danlos syndrome, osteogenesis imperfecta, calcium imbalance).
- Has a Vitamin D deficiency, defined as a 25-hydroxy Vitamin D serum concentration of ≤11ng/mL .
- Has an active malignancy or prior history of malignancy (except for basal cell carcinoma of the skin).
- Has an overt or active systemic infection (e.g., HIV/AIDS, hepatitis, bacteremia).
- Has been on oral or injectable steroids for six weeks or more at time of enrollment. This does not include episodic steroid use; inhaled steroids; or steroid medication (e.g., Epidural Steroid Injections, Medrol DosePaks) specifically for the perioperative management of symptoms.
- Has a condition requiring postoperative medications that could interfere with bone healing of the implant, such as steroids. This does not include low dose aspirin for prophylactic anticoagulation; routine perioperative anti-inflammatory drugs; episodic steroid use; or inhaled steroids.
- Has a history of certain autoimmune diseases. (Refer to the List of Autoimmune Diseases in the CIP for further information.)
- Has a history of exposure to injectable collagen or silicone implants.
- Has any previous exposure to any recombinant BMPs of either human or animal extraction.
- Has a history of hypersensitivity to collagen or protein pharmaceuticals (e.g., monoclonal antibodies or gamma globulins).
- Has a history of allergy to bovine collagen products.
- Has a documented allergy or intolerance to metal or metal alloys, such as stainless steel or titanium.
- Has chronic or acute renal and/or hepatic failure or prior history of renal and/or hepatic parenchymal disease.
- Is mentally incompetent. If questionable, obtain psychiatric consult.
- Is a prisoner.
- Is an alcohol and/or drug abuser as defined by currently undergoing treatment for alcohol and/or drug abuse.
- Has received treatment with an investigational therapy (drug, device, and/or biologic) within 28 days prior to implantation surgery or such treatment is planned during the 12-month period following the study surgery
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: INFUSE/MASTERGRAFT
Patients received INFUSE/MASTERGRAFT granules with rigid internal fixation.
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INFUSE® (rhBMP-2) on an absorbable collagen sponge (ACS) and MASTERGRAFT® granules with appropriate rigid internal fixation hardware (reamed IM nail or plate/screws)
Otros nombres:
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Comparador activo: Autograft bone
Patients received autograft bone with rigid internal fixation.
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Autogenous bone graft with appropriate rigid internal fixation hardware (reamed IM nail or plate/screws)
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Overall Success
Periodo de tiempo: 12 Months
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Overall success is reported as participants who met all of the following criteria: 1. radiographic union success; 2. success in weight bearing ability; 3. improvement in pain at the delayed healing site; 4. no serious adverse event classified as "implant-associated" or "implant/surgical procedure-associated" (device-related); 5.no additional surgical procedures classified as a failure.
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12 Months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Radiographic Union Success
Periodo de tiempo: 12 months
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Radiographic union success (a component of overall success) was defined as complete disappearance of fracture lines or the presence of bridging bone across the delayed healing site as observed on at least three of the four cortices (anterior, posterior, medial, and lateral), using plain films.
If there was more than one delayed healing fracture line, all fracture lines must have been united in order to be considered a successful fracture union.
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12 months
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Success in Weight Bearing Ability
Periodo de tiempo: 12 months
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Success in weight bearing ability (a component of overall success) was defined that subject was able to bear weight without severe pain on the affected limb.
The subject was asked to stand, bearing full weight on the affected limb in a single-leg stance without ambulatory assistance for 10 seconds.
If the subject was able to do so without severe pain, a positive (success) response was recorded.
If the subject was either unable to stand on the affected limb in a single-leg stance or declined to do so because of limb weakness, poor balance, or severe leg pain, a negative (failure) response was documented.
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12 months
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Success of Pain Status at the Delayed Healing Site
Periodo de tiempo: 12 months
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After walking five or six steps, subjects rated their intensity of pain/discomfort at the delayed healing site using a numerical rating scale from 0-10, with a score of 0 representing "no pain" and a score of 10 representing "pain as bad as it could be".
Subjects who were unable or declined to walk because of severe leg pain were considered to have a score of 10.
Success for pain at the delayed healing site was defined as at least a 2-point improvement in pain from the pre-operative score.
Success of pain status at the delayed healing site was a component of overall success.
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12 months
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Success in Short Musculoskeletal Functional Assessment (SMFA)
Periodo de tiempo: 12 months
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The SMFA is an assessment tool that measures a subject's overall function for a broad range of musculoskeletal injuries and disorders.
The SMFA results were summarized into two components, the dysfunctional index and the bother index.
Success for the SMFA assessment was defined as any improvement post-operatively as compared to the pre-operative condition.
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12 months
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Success in Short Form 36-Item (SF-36) Health Survey
Periodo de tiempo: 12 months
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SF-36 was used to assess general health status.
The SF-36 results were summarized into two components, a physical component summary (PCS) and a mental component summary (MCS).
Success was defined as any improvement in a subject's SF-36 PCS post-operatively as compared to the pre-operative condition.
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12 months
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Number of Subjects Having Additional Surgical Procedure Classified as a Treatment "Failure"
Periodo de tiempo: 12 months
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Subject who had a surgery after the original study treatment was classified as a treatment "failure" if the additional surgery or treatment occurred in the involved limb and affected the study treatment and/or its mechanism of action in relation to the diagnosis or condition of the subject that was the cause for having the original study treatment.
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12 months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de noviembre de 2010
Finalización primaria (Actual)
1 de octubre de 2013
Finalización del estudio (Actual)
1 de diciembre de 2013
Fechas de registro del estudio
Enviado por primera vez
17 de noviembre de 2009
Primero enviado que cumplió con los criterios de control de calidad
17 de noviembre de 2009
Publicado por primera vez (Estimar)
18 de noviembre de 2009
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
21 de enero de 2015
Última actualización enviada que cumplió con los criterios de control de calidad
7 de enero de 2015
Última verificación
1 de enero de 2015
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- Medtronic P07-01
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .