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Weight Change and the Risk of Chronic Pain Following Hip and Knee Arthroplasties

NCT ID: NCT06024161

Last Updated: 2023-09-06

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

UNKNOWN

Total Enrollment

6400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-11-01

Study Completion Date

2024-11-30

Brief Summary

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The study is a nationwide, register-based cohort survey study. The objective of this study is to investigate whether weight change is associated with the incidence of persistent postoperative pain following total hip arthroplasty and knee arthroplasty across non-obese and obese and patients.

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Detailed Description

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Conditions

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Persistent Postsurgical Pain Arthritis Knee Arthropathy of Knee Arthropathy of Hip Weight Loss Weight Gain Obesity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Weight gainers

Weight gain 11-15 months after arthroplasty

Weight gain

Intervention Type OTHER

≥5% weight gain

Weight losers

Weight loss11-15 months after arthroplasty

Weight loss

Intervention Type OTHER

≥5% weight loss after arthroplasty

Weight unchanged

Weight unchanged 11-15 months after arthroplasty

Weight unchanged

Intervention Type OTHER

\<5% weight change after arthroplasty

Interventions

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Weight gain

≥5% weight gain

Intervention Type OTHER

Weight loss

≥5% weight loss after arthroplasty

Intervention Type OTHER

Weight unchanged

\<5% weight change after arthroplasty

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

\- Patients operated with primary hip or knee arthroplasty for osteoarthritis 11-15 months before survey distribution

Exclusion Criteria

* Legally incompetent citizens, i.e., persons with a legal guardian, will not be asked to participate.
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bispebjerg Hospital

OTHER

Sponsor Role lead

Responsible Party

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Saber Muthanna Saber

MD, PhD fellow

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Søren Overgaard, MD,DMSc,Prof

Role: STUDY_DIRECTOR

Department of orthopedic surgery, Bispebjerg University Hospital, Denmark

Central Contacts

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Saber M. Saber, MD

Role: CONTACT

[email protected]
004521299265

Jens Laigaard, MD

Role: CONTACT

[email protected]

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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p-2023-14578

Identifier Type: -

Identifier Source: org_study_id

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