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A multi-stage randomised controlled study for the assessment of postoperative therapeutic procedures after total knee arthroplasty

A multi-stage randomised controlled study for the assessment of postoperative therapeutic procedures after total knee arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013617
Enrollment
100
Registered
2017-12-19
Start date
2017-11-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M17

Interventions

Group 1: control group with standard postoperative treatment, standard treatment is standardized by the clinic, on the first and the second postoperative day, the physiotherapeutic treatment mainly ta

Sponsors

Brandenburgische Technische Universität C-S
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 80 Years

Inclusion criteria

Inclusion criteria: For Group A, subjects aged between 22 and 27 years will be recruited at a university. Groups B .. X will be recruited at an orthopaedics department and will comprise subjects aged between 50 and 80 years who present at the department prior to a TKA operation that they are due to undergo.

Exclusion criteria

Exclusion criteria: For Group A, subjects may not have any restrictions in the function of their lower limbs. Subjects who report a medical history of injuries that might compromise symmetry will be excluded. These include fractures and cruciate ligament ruptures, but also other kinds of immobilisation in the past 24 months, such as after supination trauma or acute pain in the past three months. They may not have any diseases that are associated with neurological symptom complexes, balance disorders or muscular dystrophies. For Group B-X, subjects who cannot walk independently prior to surgery or who have serious neurological diseases or diseases of the vestibular system will be excluded.

Design outcomes

Primary

MeasureTime frame
preoperative, 9 days postoperativ and 6 weeks postoperative: 10-m walk test, time up and go, three times sit to stand, isometric maximal force with a handheld dynamometer, stair climbing test, manual leg circumference measurement; 5 days postoperativ: 10-m walk test, time up and go, three times sit to stand, isometric maximal force, manual leg circumference measurement;

Secondary

MeasureTime frame
preoperative and 6 weeks postoperative: "knee society score", "Western Ontario and McMaster Universities Osteoarthritis Index"

Countries

Germany

Contacts

Public ContactHagen Hommel

Krankenhaus Markisch-Oderland GmbH

h.hommel@khmol.de03345640401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026