Hyperpronation and Foot Pain

This study has been completed.
Information provided by (Responsible Party):
Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier:
First received: August 14, 2008
Last updated: December 10, 2015
Last verified: December 2015
Effects of training and pellots

Condition Intervention
Arthritis of Knee
Procedure: training and pellots

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Effect of Training and Pellots in Treatment of Foot Pain Caused by Hyperpronation

Resource links provided by NLM:

Further study details as provided by Northern Orthopaedic Division, Denmark:

Enrollment: 50
Study Start Date: June 2007
Study Completion Date: April 2013
Primary Completion Date: April 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
training and pellots
Procedure: training and pellots
training and pellots
No Intervention: 2


Ages Eligible for Study:   18 Years to 110 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

Exclusion Criteria:

  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00736138

Northern Orthopaedic Division, Klinik Aalborg
Aalborg, Northern Jutland, Denmark
Sponsors and Collaborators
Northern Orthopaedic Division, Denmark
Principal Investigator: Ole H Simonsen, MD Northern Orthopaedic Division
  More Information

Responsible Party: Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier: NCT00736138     History of Changes
Other Study ID Numbers: ON-02-001-OSi 
Study First Received: August 14, 2008
Last Updated: December 10, 2015
Health Authority: Denmark: The Danish National Committee on Biomedical Research Ethics
Denmark: Danish Dataprotection Agency

ClinicalTrials.gov processed this record on May 26, 2016