Purpose

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.

Condition

Eligibility

Eligible Ages
Between 18 Years and 49 Years
Eligible Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Willing and able to read and provide written informed consent. - Female in good general health, age 18-49 (inclusive). - History of regular menstrual cycles during the previous 3months lasting approximately 21-35 days, including at least 4 days of menstruation, and expecting to menstruate during the study period. - History of use of applicator tampons within the past 12 months without discomfort. - Tracks menstruation and be able to confidently predict onset of menstruation - Normally use at least 6 tampons for protection during menstruation. - Normally uses regular, super, and/or super plus absorbency tampons for menstrual protection. - Agrees to the conduct of all study procedures, including gynecological exams and agrees to follow all study instructions and return for scheduled appointments. - Has used an acceptable form of birth control for at least one month prior to enrollment and for the duration of the study.

Exclusion Criteria

  • Pregnant, lactating or is trying to become pregnant. - Less than six (6) weeks post-partum. - Has a menstrual abnormality (such as oligomenorrhea or amenorrhea). - Has a known allergy or sensitivity to components of the investigational products - Any other medical condition or history, as determined by the Investigator that could compromise the study results or subject safety.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Other
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Test Tampon
  • Device: Tampon A
    Commercially available tampons in regular, super, and super plus absorbencies

Recruiting Locations

Princeton Consumer Research
St. Petersburg, Florida 33702
Contact:
Christine Maraghy
727-576-7300
info@princetonconsumer.com

More Details

NCT ID
NCT07561905
Status
Recruiting
Sponsor
Kimberly-Clark Corporation

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.