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:
2025-12-25 @ 3:25 AM
Ignite Modification Date:
2025-12-25 @ 3:25 AM
NCT ID:
NCT01341405
Eligibility Criteria:
Inclusion Criteria:
1. Males and females, age 20 years old and more, able and willing to provide written informed consent to participate in the study
2. Confirmed osteoarthritis (OA) of the knee or hip by radiograph obtained within the past 20 years and diagnosed according to American College of Rheumatology (ACR) guidelines.
3. Subject must have pain at least 3 month duration from osteoarthritis (OA)
4. Normal blood pressure (BP) \[systolic BP 90-140 mmHg, diastolic BP 50-90 mmHg\] and heart rate (HR) \[resting 45-90 beats per minute (bpm)\]
5. Subjects with hypertension should have stably taken ACE inhibitor, angiotensin II receptor (type AT1) antagonist, beta-blocker and/or diuretics at least 3 months at the time of screening in order to keep normal blood pressure. Subjects should not change or stop hypertension drug during the study.
6. Clinical Chemistry must be within 2x normal limits
7. Urinalysis must be within normal range.
8. Prior to randomization on Day 1, the mean WOMAC pain score in the index joint must be between 4 and 8 on a 0-10 numerical rating scale.
9. Subjects and their sexual partners must agree to use double barrier contraception during the study period and for 3 months afterwards or provide proof of surgical sterility or post-menopause more than 1 year.
10. Subject must be able to read and understand and follow the study instructions.
Exclusion Criteria:
1. Use of any analgesics except the study medication or paracetamol (acetaminophen) at any time during this study;
2. Use of corticosteroids or intra-articular viscosupplementation within 3 months of screening;
3. Use of antidepressants or anticonvulsants within 2 months of screening;
4. Cognitive or psychiatric disorders, or daytime use of medications (alcohol, benzodiazepines, barbiturates, muscle relaxants) that could diminish compliance with study procedures;
5. Use of anticoagulants (aspirin, warfarin, heparin) within 2 weeks of screening;
6. Use of any medications that will affect pain perception (e.g. tranquilizers, hypnotics);
7. Hypersensitivity to non-steroidal anti-inflammatory drugs (NSAIDs), cyclooxygenase (COX)-2 inhibitors, or carbonic anhydrase inhibitors;
8. Use of oriental medicine (herbal medicine) or glucosamine within 14 days of dose administration
9. History of drug or alcohol abuse within one year prior to screening;
10. Known allergy or hypersensitivity to sulfa drugs;
11. History of congestive heart failure, ischemic heart disease, peripheral arterial disease, cerebrovascular disease or subjects who have one of these diseases;
12. Use of chemotherapy agents or history of cancer, other than non-metastatic skin cancer that has been completely excised, within five (5) years prior to the screening visit;
13. Subjects with gout, pseudogout, inflammatory arthritis, Paget's disease, chronic pain syndrome, fibromyalgia, or another major joint disease;
14. Subjects requiring knee or hip arthroplasty within 2 months of screening or anticipating any need for a surgical procedure on the index joint during the study;
15. Subjects who have had surgery on the affected joint within 6 months of screening and subjects with a prosthesis at the index joint;
16. History of seizure disorder;
17. Subjects with serious psychosocial co-morbidities;
18. Subjects with gastrointestinal, renal, hepatic, or coagulant disorder within 6 months of screening;
19. Esophageal or duodenal ulcer within 6 months of screening;
20. History of nasal polyps, bronchospasm, and urticaria;
21. Pregnant or breast-feeding;
22. Subject with genetic problem of galactose intolerance, Lapp lactose deficiency or glucose-galactose malabsorption (because celecoxib contains lactose)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Study:
NCT01341405
Study Brief:
Protocol Section:
NCT01341405