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Assessing Physical Activity Levels of Patients Following HTO.

NCT03526172 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2024-10-15

No results posted yet for this study

Summary

High tibial osteotomy (HTO is often indicated in physically active patients. The insertion of a bone graft during surgery has been shown to have good clinical and biomechanical outcomes, however objective data regarding post-surgery physical activity (PA) levels in patients who have undergone HTO with and without bone grafts does not exist in the literature.

Using accelerometers and questionnaires, this study will be the first to investigate this in an objective way.

Conditions

  • High Tibial Osteotomy With Allograft Wedge
  • High Tibial Osteotomy Without Allograft Wedge
  • Pre- and Post-operative Physical Activity Levels

Interventions

PROCEDURE

High tibial osteotomy

Uni-lateral medial opening-wedge high tibial osteotomy following a minimally invasive approach.

DEVICE

Allograft wedge

Insertion of allograft wedge into the osteotomy gap during the HTO procedure

DEVICE

Accelerometer

ActivPal accelerometer attached to thigh of patient to collect objective physical activity data at pre-determined intervals before and after surgery

OTHER

Questionnaire

Validated clinical questionnaires administered to patients to collect subjective physical activity data at pre-determined intervals before and after surgery

Sponsors & Collaborators

  • Hampshire Hospitals NHS Foundation Trust

    collaborator OTHER

  • University of Winchester

    lead OTHER

Principal Investigators

  • Simon Jobson · University of Winchester

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-26
Primary Completion
2020-05-30
Completion
2020-05-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03526172 on ClinicalTrials.gov