A Prospective Total Joint Surgery Registry to Monitor Short- and Long-Term Clinical Outcomes

NCT ID: NCT06687109

Last Updated: 2024-11-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-10

Study Completion Date

2030-01-01

Brief Summary

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The investigators propose a prospective longitudinal registry study to collect and compare preoperative and postoperative information from patients who undergo total joint arthroplasty (TJA). Outcomes will be assessed with common, routinely available patient-reported outcomes measures (PROM's) such as the HOOS Jr., Oxford score, Knee Society Score, Harris Hip Score, and other patient satisfaction and function assessments in use in Orthopedics.

Detailed Description

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The investigators propose a prospective longitudinal registry study to collect and compare preoperative and postoperative information from patients who undergo total joint arthroplasty (TJA). Outcomes will be assessed with common, routinely available patient-reported outcomes measures (PROM's) such as the HOOS Jr., Oxford score, Knee Society Score, Harris Hip Score, and other patient satisfaction and function assessments in use in Orthopedics. Investigators will also record both demographic and clinical data about the subject's history of joint pain, past treatment, medical co-morbidities, and surgical procedure.

Additionally, gait analysis and standardized physical capacity testing will be included as an option. All patients undergoing hip or knee replacement with the primary investigator will be included for data collection. All procedures and treatment will follow the standard of care, and all prosthetic implants with be FDA-approved. Data will be used to evaluate the effect on both short and long-term comfort and function of patients diagnosed with hip or knee pain who undergo joint replacement. The main purpose of the study is to provide quality improvement data on the patients in the Principal Investigator's (PI's) practice currently undergoing joint surgery. This project creates a data repository to store participants' data for this and possible future research.

Conditions

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Osteoarthritis

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Registry Knee

Total Knee Arthroplasty

Intervention Type PROCEDURE

Total Knee Arthroplasty

Registry Hip

Total Hip Arthroplasty

Intervention Type PROCEDURE

Total Hip Arthroplasty

Interventions

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Total Knee Arthroplasty

Total Knee Arthroplasty

Intervention Type PROCEDURE

Total Hip Arthroplasty

Total Hip Arthroplasty

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients who are scheduled to undergo TJA by the Principal Investigator

Exclusion Criteria

* Age \< 18
* Unable to speak and read English
* Prisoners or any other patients who, in the opinion of the investigator, are unlikely to return for follow-ups or unreliable in completing the assessments
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Spokane Joint Replacement Center

OTHER

Sponsor Role lead

Responsible Party

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David F. Scott, MD

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Spokane Joint Replacement Center

Spokane, Washington, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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David F Scott, MD

Role: CONTACT

509-466-6393 ext. 15

Annalise R McInelly, MPH

Role: CONTACT

509-466-6393 ext. 51

Facility Contacts

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Annalise R McInelly, MPH

Role: primary

509-466-6393 ext. 51

Other Identifiers

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SJRC-REG

Identifier Type: -

Identifier Source: org_study_id

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