|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0023981,
umls-concept:C0024090,
umls-concept:C0034656,
umls-concept:C0041714,
umls-concept:C0205210,
umls-concept:C0220825,
umls-concept:C0332466,
umls-concept:C0439810,
umls-concept:C0559956,
umls-concept:C1274040,
umls-concept:C1556138,
umls-concept:C1705370,
umls-concept:C2004457,
umls-concept:C2603343,
umls-concept:C2826366
|
|
pubmed:issue |
14
|
|
pubmed:dateCreated |
2005-7-18
|
|
pubmed:abstractText |
A prospective, randomized, multicenter, Food and Drug Administration-regulated Investigational Device Exemption clinical trial.
|
|
pubmed:commentsCorrections |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
1528-1159
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
|
pubmed:day |
15
|
|
pubmed:volume |
30
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1565-75; discussion E387-91
|
|
pubmed:dateRevised |
2011-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:16025024-Adult,
pubmed-meshheading:16025024-Disability Evaluation,
pubmed-meshheading:16025024-Employment,
pubmed-meshheading:16025024-Female,
pubmed-meshheading:16025024-Follow-Up Studies,
pubmed-meshheading:16025024-Humans,
pubmed-meshheading:16025024-Intervertebral Disc,
pubmed-meshheading:16025024-Intervertebral Disc Displacement,
pubmed-meshheading:16025024-Low Back Pain,
pubmed-meshheading:16025024-Lumbar Vertebrae,
pubmed-meshheading:16025024-Male,
pubmed-meshheading:16025024-Middle Aged,
pubmed-meshheading:16025024-Narcotics,
pubmed-meshheading:16025024-Pain Measurement,
pubmed-meshheading:16025024-Patient Satisfaction,
pubmed-meshheading:16025024-Prospective Studies,
pubmed-meshheading:16025024-Prostheses and Implants,
pubmed-meshheading:16025024-Prosthesis Design,
pubmed-meshheading:16025024-Spinal Fusion,
pubmed-meshheading:16025024-Treatment Outcome,
pubmed-meshheading:16025024-United States,
pubmed-meshheading:16025024-United States Food and Drug Administration
|
|
pubmed:year |
2005
|
|
pubmed:articleTitle |
A prospective, randomized, multicenter Food and Drug Administration investigational device exemptions study of lumbar total disc replacement with the CHARITE artificial disc versus lumbar fusion: part I: evaluation of clinical outcomes.
|
|
pubmed:affiliation |
Texas Back Institute, Plano, Texas 75093, USA. sblumenthal@texasback.com
|
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
|
