This is a Post-Marketing Surveillance of Quadra-P anteverted stem prosthesis.
The primary objective of this study is to evaluate the 10-year survival of the anteverted Quadra-P stem in patients operated for primary total hip arthroplasty, according to the inclusion criteria. Secondary objectives: * To assess clinical performance by Harris Hip score collected during preoperative and postoperative visits at 3 months, 1, 2, 5, 7 and 10 years. * Assess radiological performance by standard radiographic examination performed preoperatively, postoperatively before discharge and during postoperative visits at 3 months, 1, 2, 5, 7 and 10 years. * Assessing the patient's perception of the prosthetic joint by means of FJS questionnaire collected during the preoperative visit and postoperative visits at 3 months and at 1, 2, 5, 7 and 10 years after surgery. * Assessment of functional recovery by gait analysis study * Collect the rate of complications throughout the course of the study
Study Type
OBSERVATIONAL
Enrollment
300
* Assess clinical performance by Harris Hip score collected during preoperative and postoperative visits at 3 months, 1, 2, 5, 7 and 10 years. * Assess radiological performance by standard radiographic examination performed before surgery, after surgery before discharge and during postoperative visits at 3 months, 1, 2, 5, 7 and 10 years. * Assessing the patient's perception of the prosthetic joint by means of FJS questionnaire collected during the preoperative visit and postoperative visits at 3 months and at 1, 2, 5, 7 and 10 years after surgery. * Assessment of functional recovery by gait analysis study * Collect the rate of complications throughout the course of the study
Istituto Ortopedico Franco Scalabrino
Messina, Messina, Italy
Evaluate the 10-year survival of the anteverted Quadra-P stem
% survival rate
Time frame: 10 years
Assess clinical performance
Harris Hip score (HHS) (0 minimum-100 maximum)
Time frame: at 3 months, 1, 2, 5, 7 and 10 years.
Assess radiological performance
Assess radiological performance by standard radiographic examination performed before surgery, after surgery before discharge and during postoperative visits
Time frame: at pre-op, 3 months, 1, 2, 5, 7 and 10 years.
Assessing the patient's perception of the prosthetic joint
Forgotten Joint Score (FJS) (0 minimum-100 maximum)
Time frame: at 3 months and at 1, 2, 5, 7 and 10 years after surgery.
Assessment of functional recovery
Assessment of functional recovery by gait analysis study
Time frame: at pre-op, 3 months and at 1 year after surgery.
Collect the rate of complications
Collect the rate of complications throughout the course of the study
Time frame: at pre-op, immediate post-op, 3 months, 1, 2, 5, 7 and 10 years.
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