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Changes of Plantar Pressure After Knee Reconstructive Surgery (PEDKnee)

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ClinicalTrials.gov Identifier: NCT02906735
Recruitment Status : Unknown
Verified September 2016 by Harrasser, Technische Universität München.
Recruitment status was:  Recruiting
First Posted : September 20, 2016
Last Update Posted : October 19, 2016
Sponsor:
Information provided by (Responsible Party):
Harrasser, Technische Universität München

Brief Summary:
Knee reconstructive surgery (knee prosthesis, osteotomies) often results in changes of alignment of the lower limb axis. This affects also biomechanics of the hindfoot. There is a lack of understanding what changes of alignment of the lower limb causes to the ankle. The investigators want to evaluate the effects of knee surgeries onto the plantar foot pressure investigated by means of static and dynamic pedography.

Condition or disease Intervention/treatment
Knee Pain Treated With Knee Arthroplasty Procedure: Surgery

Study Type : Observational
Estimated Enrollment : 50 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of Static and Dynamic Foot Pressure Measurement After Implantation of Knee Joint Prostheses or Alignment Surgeries of the Knee
Study Start Date : September 2016
Estimated Primary Completion Date : September 2017
Estimated Study Completion Date : November 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Foot Health

Group/Cohort Intervention/treatment
Study group
Patients with knee surgery undergo plantar foot pressure measurement pre- and postoperatively
Procedure: Surgery
Implantation of knee joint prosthesis or deviation osteotomies of the knee




Primary Outcome Measures :
  1. Foot pressure curve preoperatively [ Time Frame: -1 day ]
    scale


Secondary Outcome Measures :
  1. Foot pressure curve postoperatively [ Time Frame: 1 year ]
    scale



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Patients planned for knee surgery
Criteria

Inclusion Criteria:

  • Patients planned for knee surgery willing to participate at this study

Exclusion Criteria:

  • No informed consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02906735


Contacts
Contact: Norbert Harrasser 15232716657 norbert.harrasser@gmx.net

Locations
Germany
Klinikum rechts der Isar Recruiting
Munich, Bavaria, Germany, 81675
Contact: Norbert Harrasser, DR.    00498941405229    norbert.harrasser@gmx.net   
Contact: Ingo Banke, Dr.    00498941405284    ingo@banke.eu   
Sponsors and Collaborators
Technische Universität München
Investigators
Principal Investigator: Norbert Harrasser Klinikum rechts der Isar

Responsible Party: Harrasser, Principal Investigator, Technische Universität München
ClinicalTrials.gov Identifier: NCT02906735     History of Changes
Other Study ID Numbers: TUM1
First Posted: September 20, 2016    Key Record Dates
Last Update Posted: October 19, 2016
Last Verified: September 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided