STUDY DESIGN Clinical observational study. OBJECTIVE The ROTAIO® cervical disc prosthesis is a novel unconstrained implant with a variable center of rotation aiming at physiological motion. The objective of this multicenter prospective trial was to evaluate clinical outcome and complications within 2 years. MATERIAL AND METHODS 120 patients (72 females and 48 males with median age of 43.0 years [23-60 yrs] underwent ACDA (ROTAIO®, SIGNUS Medical, Alzenau, Germany) and were prospectively followed for 24 months. Preoperative complaints were mainly associated with radiculopathy (n = 104) or myelopathy (n=16). There were 108 monosegmental and 12 bisegmental procedures including 6 hybrid constructs. Clinical outcome was evaluated ...
Objective In the present study, we present the results with at least 10 years of follow-up of the ce...
Study DesignProspective cohort study.PurposeTo study clinicoradiological parameters of zero-profile ...
Study Design: Non-randomized prospective and single center clinical trial of the ProDisc Vivo prosth...
Objective Anterior Cervical Discectomy and Arthroplasty (ACDA) is an established treatment for de...
Background: The Swiss Federal Office of Public Health demanded a nationwide HTA-registry for cervica...
OBJECTIVE The authors compared the efficacy and safety of arthroplasty using the Prestige LP cervica...
Cervical disc arthroplasty (CDA) is a safe and effective option to improve clinical outcomes (e.g., ...
Study Design. Retrospective analysis was performed on data from 251 patients that were included in t...
Anterior cervical discectomy and fusion (ACDF) has long been considered the gold standard for treati...
Background: Anterior cervical decompression and fusion (ACDF) is a common procedure in neurosurgical...
Surgical treatment for cervical radiculopathy is increasing. Treatment with motion preserving anteri...
OBJECTIVE The aim of this study was to assess long-term clinical safety and effectiveness in patient...
BACKGROUND: To investigate the efficacy of adding supplemental fusion or arthroplasty after cervical...
OBJECTIVE: The concept of accelerated degeneration of adjacent disc levels as a consequence of incre...
STUDY DESIGN: A prospective, randomized multicenter IDE trial between May 2002 and October 2004. OBJ...
Objective In the present study, we present the results with at least 10 years of follow-up of the ce...
Study DesignProspective cohort study.PurposeTo study clinicoradiological parameters of zero-profile ...
Study Design: Non-randomized prospective and single center clinical trial of the ProDisc Vivo prosth...
Objective Anterior Cervical Discectomy and Arthroplasty (ACDA) is an established treatment for de...
Background: The Swiss Federal Office of Public Health demanded a nationwide HTA-registry for cervica...
OBJECTIVE The authors compared the efficacy and safety of arthroplasty using the Prestige LP cervica...
Cervical disc arthroplasty (CDA) is a safe and effective option to improve clinical outcomes (e.g., ...
Study Design. Retrospective analysis was performed on data from 251 patients that were included in t...
Anterior cervical discectomy and fusion (ACDF) has long been considered the gold standard for treati...
Background: Anterior cervical decompression and fusion (ACDF) is a common procedure in neurosurgical...
Surgical treatment for cervical radiculopathy is increasing. Treatment with motion preserving anteri...
OBJECTIVE The aim of this study was to assess long-term clinical safety and effectiveness in patient...
BACKGROUND: To investigate the efficacy of adding supplemental fusion or arthroplasty after cervical...
OBJECTIVE: The concept of accelerated degeneration of adjacent disc levels as a consequence of incre...
STUDY DESIGN: A prospective, randomized multicenter IDE trial between May 2002 and October 2004. OBJ...
Objective In the present study, we present the results with at least 10 years of follow-up of the ce...
Study DesignProspective cohort study.PurposeTo study clinicoradiological parameters of zero-profile ...
Study Design: Non-randomized prospective and single center clinical trial of the ProDisc Vivo prosth...