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: March 28, 2014
Last verified: March 2014

August 14, 2008
March 28, 2014
June 2007
April 2013   (final data collection date for primary outcome measure)
Not Provided
Not Provided
Complete list of historical versions of study NCT00736138 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Hyperpronation and Foot Pain
Effect of Training and Pellots in Treatment of Foot Pain Caused by Hyperpronation

Effects of training and pellots

Not Provided
Interventional
Not Provided
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
Not Provided

*   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 and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00736138
ON-02-001-OSi
Not Provided
Northern Orthopaedic Division, Denmark
Northern Orthopaedic Division, Denmark
Not Provided
Principal Investigator: Ole H Simonsen, MD Northern Orthopaedic Division
Northern Orthopaedic Division, Denmark
March 2014

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