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NCT02967744 Clinical Trial

NSAID Treatment of Patients With Osteoarthritis

Osteoarthritis,Knee Clinical Trial

Official title:
BEVAR: Patientspecifik Behandling Ved Artrose - Et "Proof-of-concept"- Kvalitetssikringsstudie

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02967744
Other study ID # N-20140077
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2016
Est. completion date February 1, 2018

Study information
Verified date February 2024
Source Aalborg University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study investigates associations between pre treatment pain intensity and central pain mechanisms on the effect of 8-week treatment of NSAIDs in patients with knee osteoarthritis.

Recruitment information / eligibility
Status Completed
Enrollment 162
Est. completion date February 1, 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Diagnosed Knee Ostoarthritis Exclusion Criteria: - Current ulcer diagnosed by endoscope - Asthma or other allergic reaction to NSIADs - Kidney disease - Myocardial infarction within the last six months - Severe hyper tension (systolic =180mmHg, diastolic =110mmHg) - Severe thrombocytopenia (thrombocyst count <50x10^9/l) - Insufficience lever or kidney function

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• NSAID
NSAIDs are among the most common pain treatments for patients with osteoarthritis.

Locations
Country Name City State
Denmark Center for Sensory Motor Interaction, Aalborg University Aalborg East

Sponsors (1)
Lead Sponsor Collaborator
Aalborg University

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain intensity measured on a 10cm visual analog scale Patients will be asked to rate the pain intensity 8 weeks after treatment on a 10cm visual analog scale (0 indicating no pain, 10 indicating worst imaginable pain 8 weeks after treatment
See also
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