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 @ 10:56 PM
Ignite Modification Date:
2025-12-24 @ 10:56 PM
NCT ID:
NCT01566669
Eligibility Criteria:
Inclusion Criteria:
* women scheduled for elective gynecological surgery under combined spinal-epidural anesthesia
Exclusion Criteria:
* contraindications for CSE placement
* known allergy, sensitivity, or contraindication to opioid and nonopioid analgesic drugs
* history of bleeding disorders, peptic ulceration, or anticoagulant use within the past month
* current pregnancy or breastfeeding
* history of known or suspected drug abuse
* unable to understand the use of pain assessment scales and the PCA device
* Patient with asthma or bronchospasm, requiring treatment with glucocorticoids
* poorly controlled hypertension or diabetes, a chronic or acute renal or hepatic disorder, or inflammatory bowel disease
* patients had taken antidepressants, narcotic analgesics, antihistamines, anxiolytics, hypnotics, sedatives, NSAIDs, or corticosteroids up to 24 h before receipt of the study medication
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01566669
Study Brief:
Protocol Section:
NCT01566669