Risk of Chronic Post-surgical Pain After TKA

NCT ID: NCT06079749

Last Updated: 2023-10-12

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

COMPLETED

Total Enrollment

403 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-10-12

Study Completion Date

2022-12-31

Brief Summary

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Chronic post-surgical pain (CPSP) is a common surgical complication. The role of timing in the development of CPSP after bilateral total knee arthroplasty (BTKA) is not well studied. We aimed to compare the occurrence of CPSP in patients who underwent simultaneous or staged BTKA without discharge between procedures.

Detailed Description

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Conditions

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Bilateral Total Knee Chronic Pain Following Arthroplasty

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Simultaneous BTKA

Simultaneous BTKA

Simultaneous BTKA

Intervention Type PROCEDURE

Simultaneous BTKA

Staged BTKA

Staged BTKA

Staged BTKA

Intervention Type PROCEDURE

Staged BTKA

Interventions

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Simultaneous BTKA

Simultaneous BTKA

Intervention Type PROCEDURE

Staged BTKA

Staged BTKA

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* From October 12, 2012 to December 2, 2021, patients who underwent bilateral or staged knee replacement surgery during a single hospitalization under Professor Lee Woo-seok at the Department of Orthopedics at Gangnam Severance Hospital due to bilateral knee arthritis.

Exclusion Criteria

* Patients whose post-operative pain information cannot be confirmed through outpatient visit records 1 year after surgery
* Those who have undergone surgery other than knee arthritis surgery within 1 year after surgery
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Gangnam Severance Hospital

OTHER

Sponsor Role lead

Responsible Party

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Do-Hyeong Kim

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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3-2023-0080

Identifier Type: -

Identifier Source: org_study_id

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