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 @ 11:10 PM
Ignite Modification Date:
2025-12-24 @ 11:10 PM
NCT ID:
NCT07048769
Eligibility Criteria:
Inclusion Criteria:
* Undergoing uterine cavity and tubal patency evaluation via saline infusion sonogram with balloon catheter at Montefiore Institute for Reproductive Medicine and Health
* Pre-medicated with 600-800 mg ibuprofen taken 30 minutes to 4 hours prior to procedure
* Able to provide informed consent in English or Spanish
* Capacity to consent
Exclusion Criteria:
* Undergoing uterine cavity evaluation only (without tubal patency assessment)
* No ibuprofen pre-medication prior to procedure
* Received misoprostol within 24 hours prior to procedure
* Known allergy to lidocaine
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT07048769
Study Brief:
Protocol Section:
NCT07048769