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Clinical Trials/JPRN-UMIN000031726
JPRN-UMIN000031726
Completed
N/A

Accelerometer-Based Navigation Versus Conventional Alignment Guide for Acetabular Component Placement in Total Hip Arthroplasty: A Randomized, Controlled Trial: Comparisons of computed tomographic outcomes and liner-to-neck clearances during weight-bearing activities - Evaluation of three-dimensional kinematics after primary THA: comparison of accelerometer-based portable navigation system and conventional technique

Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University0 sites60 target enrollmentMarch 14, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Secondary osteoarthritis caused by hip dysplasia or osteonecrosis of the femoral head
Sponsor
Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 14, 2018
End Date
March 31, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patients with immature bone structure 2\) Patients with the loss of abduction muscle in affected leg 3\) Patients with insufficient bone mineral density (e.g. Corticosteroid\-induced metabolic bone disease) 4\) Patients with insufficient skin covering around the hip joint 5\) Patients with neuromuscular disease (e.g. Charcot disease) in affected leg 6\) Patients with the infection (e.g. osteomyelitis in proximal femur or purulent infection in the hip joint) 7\) Patients with stovepipe\-like femur 8\) Patients with radiation osteonecrosis of acetabulum 9\) Patients with systemic or local infection 10\) Patients with vascular interruption in affected leg 11\) Patients without the ability of walking at the postoperative time 12\) Suspicious patients with metal allergy 13\) Pregnant patients, pregnant suspicious patients, or patients who hope for pregnancy 14\) Patients with the disease which can affect consent or evaluation of the study, including dementia, schizophrenia, depression, panic disorder, or generalized anxiety disorder 15\) Patients who need to undergo the lower extremity surgery within six months after participating in the study, including total hip arthroplasty and total knee arthroplasty 16\) Patients who underwent the lower extremity surgery within six months before participating in the study, including total hip arthroplasty, total knee arthroplasty, or osteotomy 17\) Patients who doctors judged unsuitable for the study

Outcomes

Primary Outcomes

Not specified

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