Pubic Hair and the Urinary and Vaginal Microbiome
Effects of Pubic Hair Grooming on Urinary and Vaginal Microbiome
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Northwestern University
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Pre-menopausal women between the ages of 18-50
- English-speaking
- Women with either natural growth/distribution of pubic hair or complete removal of pubic hair through a reversible process.
- Women who do not feel they have urinary or vaginal health problems and are not seeking care for these issues
- Women must be willing and able to complete study documentation and study procedures.
Exclusion Criteria: Women will be excluded for any of the following:
- Hair has been removed through an irreversible process like laser or electrolysis
- Patient feels they have bothersome urinary or pelvic floor conditions for which they are seeking care (for example: vaginal prolapse, frequent urinary incontinence, chronic pelvic pain, bladder pain)
- Patient plans on having any type of surgery in the next 2 months (due to likely antibiotic use)
- Patient has a history of a transplant and is on immunosuppression
- Patient has cancer for which she is currently getting chemotherapy or radiation
- Currently taking or has taken antibiotics in the last 7 days for any reason
- Patient has symptoms of a urinary tract or vaginal infection or is found on exam or culture to have a urinary tract infection or vaginal infection
- Patient is pregnant or breastfeeding
- Patient has douched in the last 48 hours
- Patient has had intercourse in the last 48 hours
- Patient is currently menstruating
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Other: Natural Pubic Hair
Participant with natural hair crosses over to removed pubic hair
|
Natural pubic hair to fully removed pubic hair
|
|
Other: Removed Pubic Hair
Participant with no pubic hair crosses over to natural pubic hair
|
Removed pubic hair to natural pubic hair
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of Urinary and Vaginal Microbiomes
Time Frame: up to 3 months
|
Describe and compare the urinary and vaginal microbiome in the same woman with natural pubic hair and with fully removed pubic hair
|
up to 3 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Questionnaire Comparison
Time Frame: up to 3 months
|
To compare questionnaire results for standardized patient surveys in the same woman with and without pubic hair
|
up to 3 months
|
|
Self-Reported Infections
Time Frame: up to 3 months
|
Comparing self-reported vaginal infections and urinary tract infections between women who have natural pubic hair and women who fully remove their pubic hair
|
up to 3 months
|
|
Subtracting Microbiome Results
Time Frame: up to 3 months
|
To suggest whether the transurethral urinary microbiome can be determined by subtracting the vaginal microbiome from the voided urinary microbiome
|
up to 3 months
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Margaret G Mueller, MD, Northwestern University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- STU00205206
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Healthy
-
NCT06818032RecruitingHealthy | Healthy Volunteers | Healthy Subjects | Healthy Volunteer | Healthy Adult | Healthy Volunteers Only | Healthy Male and Female Subjects | Healthy Non-smokers
-
NCT07232121RecruitingHealthy | Healthy Participants | Healthy Adult Females | Volunteer | Healthy Adult Male
-
NCT07197047CompletedHealthy | Healthy Volunteers | Healthy Subjects | Healthy Participants | Static Stretching | Stretch | Stretching
-
NCT05361343RecruitingHealthy Aging | Healthy Diet | Healthy Lifestyle
-
NCT05218980Not yet recruitingHealth-related Benefits of Introducing Table Olives Into the Diet of Young Adults: Olives For HealthHealthy Diet | Healthy Lifestyle | Healthy Nutrition | Cholesterol
-
NCT07515417Active, not recruitingHealthy | Healthy Participants | Healthy Adult | Healthy Women | Healthy Adult Females | Healthy Adult Participants | Healthy Young Adults | Healthy Adult Female Participants | Healthy Adult Male | Poor Sleep Quality
-
NCT07520474CompletedHealthy Participants | Healthy Adult Participants | Healthy Young Adults
-
NCT03278535CompletedHealthy Volunteers | Healthy Subjects | Healthy Adults
-
NCT07597928Not yet recruiting
-
NCT07285122RecruitingHealthy | Healthy Smoker
Clinical Trials on No pubic hair
-
NCT06656208CompletedSacroiliac Joint Dysfunction
-
NCT04251923UnknownQuality of Life | Stress Urinary Incontinence | Vaginal Hysterectomy
-
NCT07287579Not yet recruiting
-
NCT06362941Completed
-
NCT06646146Not yet recruitingLocalized Scleroderma | Fat Grafting | Hair Transplantation
-
NCT07227883RecruitingRejuvenation | Stem Cell | Facial Aging | Stem Cell Banking
-
NCT06406621Recruiting
-
NCT06376409Completed