Adult Acquired Flatfoot Clinical Trial
Official title:
A Randomized, Prospective, Controlled Trial for Lateral Column Lengthening in Adult Acquired Flatfoot Using Biofoam Porous Metal Compared With Allograft
The purpose of this study is to compare the clinical and radiographic outcomes of a
randomized, consecutive series of adult patients, with an acquired flatfoot, treated with a
lateral column lengthening using an allograft bone wedge versus a titanium porous metal
implant (Biofoam, Wright Medical).
Null hypothesis: At six months postoperatively, there is no difference in the degree of
correction as measured by the talonavicular coverage angle between patients randomized to
allograft and Biofoam.
Alternative hypothesis: At six months postoperatively, the degree of correction as measured
by the talonavicular coverage angle will be less in patients randomized to allograft than
the degree of correction in patients randomized to Biofoam.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | June 2011 |
| Est. primary completion date | June 2011 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 25 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - Ages 25-75 - Unresponsive to conservative treatment - Patient with acquired flatfoot deformity, who is a candidate for lateral column lengthening (Stage IIB) = (greater than > 40% uncoverage of talar head by navicular on standing AP radiograph) Exclusion Criteria: - Less than 25 years of age and greater than 75 years - Pre-existing infection - Peripheral neuropathy - Charcot arthropathy - Peripheral vascular disease - Rhematoid Arthritis (RA) or inflammatory arthropathy - Metal allergy or sensitivity to metal |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | OrthoCarolina, P.A. | Charlotte | North Carolina |
| Lead Sponsor | Collaborator |
|---|---|
| OrthoCarolina Research Institute, Inc. | Wright Medical Technology |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The degree of correction as measured by talonavicular coverage angle, which is used to quantify the degree of deformity. Degree of correction is defined as the difference between the preoperative and postoperative talonavicular coverage angle. | 2 weeks, 6 weeks, 12 weeks, and 6 months | No | |
| Secondary | American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Score | 2 weeks, 6 weeks, 3 months, and 6 months | No | |
| Secondary | Foot Function Index (FFI) Score | 2 weeks, 6 weeks, 3 months, and 6 months | No | |
| Secondary | Pain Visual Analog Scale (VAS) | 2 weeks, 6 weeks, 3 months, and 6 months | No | |
| Secondary | Implant failure | 2 weeks, 6 weeks, 3 months, and 6 months | No |