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:
NCT07132151
Eligibility Criteria:
Inclusion Criteria:
* Age between 18-45 years
* ASA status Ⅰ to Ⅱ
* Diagnosed with early intrauterine pregnancy
* Body mass index (BMI) between 18 to 28 kg/m2
Exclusion Criteria:
* History of cardiac, hepatic, renal, or metabolic disorders (e.g., diabetes, hypertension, sleep apnea)
* Known allergy to opioids or ciprofloxacin components
* Cachexia
* History of substance or alcohol abuse
* ASA class III or higher
* Participation in any other drug clinical trial within the past 3 months
* Long-term use of sedative or analgesic medications
* History of neurological disorders and convulsions
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07132151
Study Brief:
Protocol Section:
NCT07132151