Clinical Trials Directory

Trials / Terminated

TerminatedNCT02239406

Acetabular Bone Vascularity in Metal-on-Metal Revisions

Status
Terminated
Phase
Study type
Observational
Enrollment
7 (actual)
Sponsor
OrthoCarolina Research Institute, Inc. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if avascular necrosis of the acetabulum is present in metal-on-metal revisions and to what depth this dead avascular bone occurs. A convenient sample of a consecutive series of 15 patients treated for metal on metal acetabular revision surgery will be included.

Detailed description

Patients being treated for metal on metal acetabular revision surgery by a physician at OrthoCarolina, PA will be screened for eligibility. These patients will be approached by their surgeon and asked to volunteer their participation in the study. Potential subjects will meet with a research coordinator to discuss details of the study and those you volunteer participation will be asked to sign an informed consent prior to the collection of study data. . Basic demographic information (initials, age, gender, height, weight, BMI), dates of original index surgery, reason for revision, type of implant being removed, and standard of care cobalt and chromium metal ion levels will be collected via chart review. Patients who meet all eligibility criteria will have three biopsies performed at the time of their revision surgery. A pathologist will note the presence or absence of bone necrosis and will measure the length (mm) of necrosis, acute inflammation, chronic inflammation, normal bone, and entire bone specimen in order to obtain a ratio. Biopsy Protocol: A bone biopsy is a procedure in which bone samples are removed (with a special instrument during surgery) and looked at under a microscope for necrosis (tissue death), infection, or other bone disorders. Once the acetabular hip replacement implants have been removed the following steps will occur: * The biopsy needle will be inserted into the bone (3 locations; 2 from ilium, 1 from pubis or ischium = 3 total). * The biopsy needle will be withdrawn and firm pressure will be applied to the biopsy site for a few minutes, until the bleeding has stopped. * Each bone biopsy sample will be labeled sequentially and by anatomic location (i.e., ilium #1, ilium #2) * The normal bone will be marked on the bone sample. * The bone biopsy sample will be sent to the lab for examination. * The acetabulum bone will be reamed so the new implant can be seated.

Conditions

Timeline

Start date
2014-11-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2014-09-12
Last updated
2016-07-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02239406. Inclusion in this directory is not an endorsement.