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 @ 11:33 PM
Ignite Modification Date:
2025-12-24 @ 11:33 PM
NCT ID:
NCT02461056
Eligibility Criteria:
Inclusion Criteria:
* American Society of Anesthesiologists (ASA) physical status І or ІІ who were able to communicate and understand the pain scales
Exclusion Criteria:
* any contraindication to the use of ibuprofen or hydromorphone
* a history of allergy or hypersensitivity
* a calculated creatinine clearance of \<75 mL/min
* the presence or history of asthma, bleeding tendency, coronary artery bypass graft (CABG) surgery, heart failure, peptic ulcer disease, inflammatory bowel disease or any other gastrointestinal disorder, and renal or hepatic disease
* pregnancy
* age younger than 18 yr
* intraoperative use of regional anesthesia
* intraoperative administration of analgesics other than remifentanil
* postoperative pain ≤3 on a NRS in the post-anesthesia care unit (PACU)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
19 Years
Maximum Age:
80 Years
Study:
NCT02461056
Study Brief:
Protocol Section:
NCT02461056