Hyperpronation and Foot Pain
Primary Purpose
Arthritis of Knee
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
training and pellots
Sponsored by

About this trial
This is an interventional treatment trial for Arthritis of Knee
Eligibility Criteria
Inclusion Criteria:
-
Exclusion Criteria:
-
Sites / Locations
- Northern Orthopaedic Division, Klinik Aalborg
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
1
2
Arm Description
training and pellots
control
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00736138
First Posted
August 14, 2008
Last Updated
December 10, 2015
Sponsor
Northern Orthopaedic Division, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT00736138
Brief Title
Hyperpronation and Foot Pain
Official Title
Effect of Training and Pellots in Treatment of Foot Pain Caused by Hyperpronation
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Northern Orthopaedic Division, Denmark
4. Oversight
5. Study Description
Brief Summary
Effects of training and pellots
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthritis of Knee
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
training and pellots
Arm Title
2
Arm Type
No Intervention
Arm Description
control
Intervention Type
Procedure
Intervention Name(s)
training and pellots
Intervention Description
training and pellots
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
-
Exclusion Criteria:
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ole H Simonsen, MD
Organizational Affiliation
Northern Orthopaedic Division
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northern Orthopaedic Division, Klinik Aalborg
City
Aalborg
State/Province
Northern Jutland
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Hyperpronation and Foot Pain
We'll reach out to this number within 24 hrs