Evaluation of Weight Bearing After Total Hip and Knee Replacement

NCT ID: NCT01135160

Last Updated: 2024-10-18

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

TERMINATED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-11-30

Study Completion Date

2022-12-31

Brief Summary

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The regime in the aftercare after total hip and knee arthroplasty(THA/TKA) differs a lot between orthopedic surgeons concerning weight bearing. The type of implant and the way of implants' anchoring are considered.

In the literature there is no data so far about the way patient take care of the recommended weight bearing during the first 6 weeks after THA and TKA.

Over a one year period starting August 2010 all patients undergoing TKA or THA at the investigators institution will have a technical device in their shoes (sole) to measure the load in each step they do in these shoes during the first 6 weeks. Patients are asked to fill out a standardised pain protocol every day (VAS) and document need of pain medication. The investigators recommend 20kg of weight on the operated leg for 6 weeks and full weight bearing at the end of week six.

The investigators believe that patients will adjust weight bearing to their level of pain and not to their surgeons recommendations.

Detailed Description

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Conditions

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Arthropathy of Hip Arthropathy of Knee

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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TKA/THA

All patients receiving TKA/THA meeting inclusion but not exclusion criteria

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* received a THA or TKA in the mentioned period of time
* is able to walk on crutches
* is able to understand our recommendations
* signed informed consent

Exclusion Criteria

* not able to walk on crutches
* not able to understand our recommendations
* other deformities of lower limbs
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kantonsspital Münsterlingen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Michael Schueler, Dr. med.

Role: PRINCIPAL_INVESTIGATOR

Chief of the department for orthopedic surgery Kantonsspital Münsterlingen, Schweiz

Locations

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Kantonsspital Münsterlingen

Münsterlingen, Thurgau, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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KSM 2010-1

Identifier Type: -

Identifier Source: org_study_id

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