Total Hip Arthroplasty Clinical Trial
Official title:
Functional Recovery After Monolateral or Bilateral Total Hip Arthroplasty
This is an observational prospective study aimed to assess the lower limbs motor and functional recovery in patients who underwent to unilateral THA respect to simultaneous bilateral THA, in early postoperative phase.
Introduction: Total hip arthroplasty (THA) represents a successful treatment for several hip
joint pathologies. In case of bilateral hip joint involvement, the advancements in surgical
techniques have made the development of bilateral THA surgery possible through one-stage
procedure. This approach seems to be as safe as unilateral THA and safer than two-stage
bilateral THA, but few studies considering functional outcomes in these patients without
exploring outcomes linked to their motor and functional performance.
Objective: the aim of the study is to assess the lower limbs motor and functional recovery in
patients who underwent to unilateral THA respect to simultaneous bilateral THA, in early
postoperative phase.
Methods: 20 patients underwent to unilateral THA and 20 patients underwent to simultaneous
bilateral THA will be recruited in the study. The partecipants will be aged from 40 to 65
years old, they will be undergone to primary THA for arthritis and the will be able to walk
for 50 m without aids. Patients with severe dysplasia (Crowe III and IV), anchylosis,
sub-anchylosis or surgical fusion of the coxophemoral joint, with traumatic event, or
previous femoral and / or pelvic osteotomy, will be excluded from the study. Weight
distribution and postural stability will be evaluated asking to participants to stay on two
stabilometric platform with open eyes and closed eyes for 45 seconds. Gait analysis will be
used to evaluate the spatio-temporal gait parametres and the ankle, knee, hip and pelvic
kinematic. Pain during walking and patients' walking ability will be also evaluated throught
Numeric Rating Scale (NRS) and Timed Up and Go test (TUG). Outcome measures will be collected
the day before surgery, after three, seven and about forty days after surgery, except for
gait analysis and Time Up and Go tests, which will not be recorded after three days.
Statistical analysis: normality and homogeneity of demographic variables and outcome measures
at the baseline will be verified. Intergroup and intra-group post-intervention differences
related to outcome measures will be investigated through ANOVA for repeated measurements
including post hoc analysis.
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