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 @ 1:45 AM
Ignite Modification Date:
2025-12-25 @ 1:45 AM
NCT ID:
NCT03067194
Eligibility Criteria:
Inclusion Criteria:
* Agreement with written informed consent and 19 years of age and older
* Patients history of OA of hand according to ACR criteria
* The 100mm Pain VAS is over 40mm
Exclusion Criteria:
* History of OA of hand surgery
* Intra-articular injections within 3 months
* History of OA of hand infections within 3 months
* Who had taken a drug that has a control of result in clinical trial by investigator's decision
* Pregnant women, nursing mothers or Fertile women who not practice contraception with appropriate methods
* clinically significant hepatic, renal, cardiovascular diseases
* Any history of adverse reaction to the study drugs
* Patients with gastrointestinal ulcers or bleeding disorders
* Finger joint injury within 6 months
* Who had following results after examination
1. K ≥ 5.5mEq/L
2. eGFR ≤ 30ml/min/1.73m\^2
* Patients on any other clinical trial or experimental treatment in the past 3 months
* Taking narcotic analgesics or patches
* History of drug abuse or alcoholism
* Who has Galactose intolerance, LAPP lactose intolerance, glucose-galactose malabsorption or genetic disorders
* An impossible one who participates in clinical trial by investigator's decision
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT03067194
Study Brief:
Protocol Section:
NCT03067194