Hyperpronation and Foot Pain

Arthritis of Knee Clinical Trial

Official title:

Effect of Training and Pellots in Treatment of Foot Pain Caused by Hyperpronation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00736138
• Other study ID #: ON-02-001-OSi
• Status: Completed
• Phase: N/A
• First received: August 14, 2008
• Last updated: December 10, 2015
• Start date: June 2007
• Est. completion date: April 2013

Study information

• Verified date: December 2015
• Source: Northern Orthopaedic Division, Denmark
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: The Danish National Committee on Biomedical Research EthicsDenmark: Danish Dataprotection Agency
• Study type: Interventional

Clinical Trial Summary

Effects of training and pellots

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: April 2013
• Est. primary completion date: April 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 110 Years

Eligibility

Inclusion Criteria:

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Arthritis of Knee

Intervention

Procedure:
• training and pellots
training and pellots

Locations

Country	Name	City	State
Denmark	Northern Orthopaedic Division, Klinik Aalborg	Aalborg	Northern Jutland

Sponsors (1)

Lead Sponsor	Collaborator
Northern Orthopaedic Division, Denmark

Country where clinical trial is conducted

Denmark,