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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02358707
Other study ID # BAP
Secondary ID
Status Recruiting
Phase N/A
First received January 15, 2015
Last updated February 6, 2015
Start date May 2014
Est. completion date May 2015

Study information

Verified date February 2015
Source Cukurova University
Contact Bayram Kelle
Phone 9003223386060-3161
Email bayramkelle@yahoo.com
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial Summary

The specimens from patients as knee osteoarthritis diagnosed who was applied ibuprofen phonophoresis will be analyzed.


Recruitment information / eligibility

Status Recruiting
Enrollment 18
Est. completion date May 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- having diagnosed as osteoarthritis

Exclusion Criteria:

- surgery at knee

- trauma at knee

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Ibuprofen phonophoresis


Locations

Country Name City State
Turkey Çukurova Üniversitesi Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary level of ibuprofen in bone by Microextraction and HPLC (High Liquid Pressure Chromatography) Effectiveness and safety 1 year Yes
Primary level of ibuprofen in synovial membrana by Microextraction and HPLC (High Liquid Pressure Chromatography) Effectiveness and safety 1 year Yes
Primary level of ibuprofen in synovial fluid by Microextraction and HPLC (High Liquid Pressure Chromatography) Effectiveness and safety 1 year Yes
Secondary Visual Analog Scale (VAS) VAS score after phonophoresis treatment 1 year Yes
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