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Clinical Trials/ISRCTN87127065
ISRCTN87127065
Completed
Phase 3

A randomised controlled trial of the effect of a two-layer compression bandage system on knee function following total knee arthroplasty

orthumbria Healthcare NHS Foundation Trust0 sites2,338 target enrollmentFebruary 20, 2017
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ConditionsSpecialty: Musculoskeletal disorders, Primary sub-specialty: Elective Orthopaedic SurgeryUKCRC code/ Disease: Musculoskeletal/ Other joint disordersMusculoskeletal DiseasesKnee arthritis/total knee replacement

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Specialty: Musculoskeletal disorders, Primary sub-specialty: Elective Orthopaedic Surgery
Sponsor
orthumbria Healthcare NHS Foundation Trust
Enrollment
2338
Status
Completed
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31068223 protocol (added 10/05/2019) 2020 Other publications in https://pubmed.ncbi.nlm.nih.gov/35600143/ An embedded randomised controlled retention trial of personalised text messages compared to non-personalised text messages in an orthopaedic setting (added 31/10/2022)

Registry
who.int
Start Date
February 20, 2017
End Date
November 7, 2020
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
orthumbria Healthcare NHS Foundation Trust

Eligibility Criteria

Inclusion Criteria

  • •1\. Patients scheduled for primary total knee arthroplasty
  • •2\. Presenting at a participating trial site
  • •3\. Aged over 18
  • •4\. Able to provide written informed consent

Exclusion Criteria

  • •1\. Unable to consent
  • •2\. History of peripheral vascular disease
  • •3\. History of peripheral neuropathy
  • •4\. History of, or current venous ulceration
  • •5\. Absent foot pulses
  • •6\. Planned same day discharge joint replacement patients
  • •7\. Revision knee arthroplasty
  • •8\. Unicondylar or patellofemoral joint knee arthroplasty
  • •9\. Regular concomitant high dose anti\-coagulant medication. Patients on routine thromboprophylaxis can be included
  • •10\. Unwilling to provide informed consent

Outcomes

Primary Outcomes

Not specified

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