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 @ 6:30 PM
Ignite Modification Date:
2025-12-24 @ 6:30 PM
NCT ID:
NCT05955768
Eligibility Criteria:
Inclusion Criteria:
1. Age ≥18 and \<65 years old;
2. Voluntary request for removal of intrauterine device under local anesthesia;
3. No known allergic reactions or sensitivity to lidocaine, physiological saline and polyvinyl formaldehyde polymer materials in the past;
4. Volunteer participation in this study.
Exclusion Criteria:
1. Dysplasia of uterine cavity structure;
2. Known lesions such as uterine fibroids that compress and cause uterine cavity deformation;
3. Presence of untreated acute cervicitis or pelvic inflammatory diseases;
4. History of cervical surgery;
5. Systemic diseases that can affect pain perception;
6. Current or past use of illegal drugs or anesthetic and analgesic drugs;
7. Unable to understand how to score pain using Visual Analog Scale (short for VAS).
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT05955768
Study Brief:
Protocol Section:
NCT05955768