Hyperpronation and Foot Pain

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier:
NCT00736138
First received: August 14, 2008
Last updated: December 10, 2015
Last verified: December 2015

August 14, 2008
December 10, 2015
June 2007
April 2013   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00736138 on ClinicalTrials.gov Archive Site
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Hyperpronation and Foot Pain
Effect of Training and Pellots in Treatment of Foot Pain Caused by Hyperpronation
Effects of training and pellots
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Interventional
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Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Arthritis of Knee
Procedure: training and pellots
training and pellots
  • Active Comparator: 1
    training and pellots
    Intervention: Procedure: training and pellots
  • No Intervention: 2
    control
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
April 2013
April 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

Exclusion Criteria:

Both
18 Years to 110 Years
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00736138
ON-02-001-OSi
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Northern Orthopaedic Division, Denmark
Northern Orthopaedic Division, Denmark
Not Provided
Principal Investigator: Ole H Simonsen, MD Northern Orthopaedic Division
Northern Orthopaedic Division, Denmark
December 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP