Suspended

Clinical Outcomes of Joint Arthroplasty

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Procedure Data

+ procedure Data

+ procedure Data

Collected from today forward - Prospective
ProcedureDevice
Who is being recruted

Rheumatic Diseases+2

+ Arthritis

+ Joint Diseases

Over 21 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: October 2012
See protocol details

Summary

Principal SponsorNorthwest Surgical Specialists, Vancouver
Last updated: September 26, 2018
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2012

Actual date on which the first participant was enrolled.

The objective of this study is to document the demographic and clinical characteristics and the long-term clinical outcomes of patients who require a robot assisted knee arthroplasty. The hypothesis is that MAKO® robot assisted surgery replacing one or two compartments of the knee joint has 10 year implant survival and clinical outcomes that are equivalent to other knee replacement systems.

NCT01705366
Principal SponsorNorthwest Surgical Specialists, Vancouver
Last updated: September 26, 2018
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

316 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 21 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Rheumatic DiseasesArthritisJoint DiseasesMusculoskeletal DiseasesOsteoarthritis

Criteria

2 inclusion criteria required to participate
has failed non-operative management of their joint disease
requires either primary or revision knee replacement surgery because of pain and joint stiffness that interferes with performance of normal daily activities
2 exclusion criteria prevent from participating
cognitively unable to complete study health-related quality of life forms
pregnant women

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Rebound Orthopedics and Neurosurgery

Vancouver, United StatesOpen Rebound Orthopedics and Neurosurgery in Google Maps
SuspendedOne Study Center