MedPath

Prospective i-FactorTM Analysis Fusion Rate and Quality of Life

Not Applicable
Not yet recruiting
Conditions
Bone Graft
Spinal Deformity
Fusion Rate
Quality of Life
Interventions
Biological: i-FactorTM Bone graft
Registration Number
NCT04610021
Lead Sponsor
Complejo Asistencial Universitario de León Urgencias
Brief Summary

Adult spinal deformity surgery is a complex procedure that involves many risks and complications. Bone grafts and bone substitutes are essential to achieve fusion and manage stability in spinal surgery.

Autologous bone has been considered the "gold-standard" for obtaining a spinal fusion. However, the source from which to obtain it is limited. Furthermore, the problems of bone quality in patients with osteoporosis and the morbidity have forced the orthopedic community to seek other options.

I-Factor ™ Bone Graft (Cerapedics, Inc., Westminster, CO) is a compound formed by peptide P-15 bound to an anorganic bone mineral of bovine origin that is composed of porous and smooth hydroxyapatite (ABM) particles.

In the literature there are no articles which identify bone formation with the i-Factor ™ graft in more than 4 instrumented levels, therefore the development of this study will allow assessing the fusion rate and quality of life of patients, which could lead to an improvement in the management and decision-making of surgical procedures, as well as better control of healthcare spending

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
128
Inclusion Criteria
  • Patients of legal age.
  • Patients diagnosed with adult deformity, whether due to scoliosis, imbalance, thoracolumbar curves, etc. In which the minimum number of levels to be instrumented is 5, that is, 4 intervertebral discs.
  • Patients who provide their informed consent in writing. (In the event that the patient's circumstances do not allow him to grant consent, this may be provided by the legal representative).
  • Present radiological tests, computed tomography and / or magnetic resonance imaging prior to surgery.
  • The implants used in the surgery are Cobalt Chrome bars and Titanium screws and interbody cages.
Exclusion Criteria
  • Patients who are expected to be unavailable for follow-up.
  • Patients with mental disabilities that make it difficult for them to fill in the questionnaires.
  • Patients who have had other types of implants placed, other than Cobalt Chrome bars and Titanium screws and interbody cages.
  • Patients who are going to have cemented and / or expansive screws, Peek boxes or another type of material other than Titanium.
  • Underlying neurological or neuromuscular disease.
  • Underlying inflammatory or tumor disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
i-Factori-FactorTM Bone graftI-Factor group: autologous bone + bench bone + i-Factor™ bone graft
Primary Outcome Measures
NameTimeMethod
Fusion rate2 years

The success of the fusion at 12 and 24 months will be determined by a specialized radiologist by the evidence in the CT scan of trabecular bone bridges between the inter-transverse areas of the vertebral bodies and the absence of radiolucency adjacent to the implants.

Minimal Clinically Important Difference (MCID)2 years

Minimal clinically important difference is defined a smallest clinical change that is important to the patient.

Short Form Health Survey-12 General Quality of life questionnaire2 years

The questions that follow ask what you think about your health. Your answers will allow you to know how you are and to what extent you are able to do your usual activities.

Patients improve when the puntuation is more than 50.

Owestry disability index2 years

Disability index questionnaire

Maximun value=100 Minimun value=0

Patients improve when this index is arround 0

VISUAL ANALOGUE SCALE2 years

Is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured.

Maximun value=10 Minimun value=0

Patients improve when this index is arround 0

Scoliosis Research Society (SRS-22)2 years

Scoliosis reseach society questionnaire

22 questions 5 options Dimensions Pain Function Selfimage Mental Health Satrisfaction

Puntuation for item and test: 1(worse) - 5(better)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CAULE

🇪🇸

León, Spain

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