The goal of this clinical trial is to confirm the safety of a tampon in healthy female volunteers. Participants will use the study tampons as they normally would for one menstrual cycle. Gynecological exams will be conducted before and after the menstrual cycle.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
60
Commercially available tampons in regular, super, and super plus absorbencies
Princeton Consumer Research
St. Petersburg, Florida, United States
RECRUITINGIncidence of Tampon Related Adverse Events
Frequency and severity of tampon related adverse events
Time frame: From enrollment to 7 days post last visit
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.