Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:40 PM
Ignite Modification Date:
2025-12-24 @ 11:40 PM
NCT ID:
NCT00794651
Eligibility Criteria:
Inclusion Criteria:
* Subject is 50 years of age or older and has osteoarthritis of the knee.
* Subject is able to communicate meaningfully in English and comply with all study procedures.
* Subject is willing to voluntarily sign and date an informed consent form, approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC), prior to the conduct of any study-specific procedures.
* Subject has experienced a minimum duration of pain of at least 6 months.
* For each of the last 15 days, pain level has remained at least a 3 on a Pain Intensity Numerical Rating (P-NRS) scale from 0 to 10; 0 means "no pain" and 10 means "worst pain imaginable".
* Subject is ambulatory.
* Subject has a primary diagnosis of osteoarthritis of the knee by medical history.
* Subject must be willing to abstain from any pain medicine for 12 hours prior to the study.
Exclusion Criteria:
* • Subject is pregnant and/or breast-feeding.
* Subject has a medical condition, other than OA, that is not well-controlled with treatment; or the subject has any clinically significant condition that would, in the opinion of the investigator, preclude study participation or interfere with the assessment of pain and other symptoms of OA.
* Subject is not able to hold a stylus or pen.
* Subject is not able to read a computer screen.
* Subject has any chronic pain syndrome (e.g., fibromyalgia) that, in the investigator's opinion, would interfere with the assessment of pain and/or other symptoms of OA.
* In the judgment of the investigator, the subject has a psychiatric or psychological disorder that would interfere with the completion of the study, confound the study results or pose patient risk.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
50 Years
Maximum Age:
85 Years
Study:
NCT00794651
Study Brief:
Protocol Section:
NCT00794651