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Prebiotic Device

PreBioGyn Gel for User Acceptability of Gel Delivery System

N/A

Waitlist Available

Led By Joanna Ellington, PhD

Research Sponsored by Glyciome, LLC

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 1 hour

Awards & highlights

Study Summary

This trial will compare PreBioGyn to other vaginal pH buffering gels, and will evaluate factors such as vaginal lubricity, smell, and applicator design.

Eligible Conditions

User Acceptability of Gel Delivery System
Sensory Perceptual Disorders

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 1 hour

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~1 hour

This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 hour for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Sensory perceptual characteristics of gels based on forearm testing

User acceptability of gel delivery system

Trial Design

3Treatment groups

Experimental Treatment

Active Control

Group I: PreBioGyn GelExperimental Treatment1 Intervention

Topical administration to forearm

Group II: Trimosan GelActive Control1 Intervention

Topical administration to forearm

Group III: RepHresh GelActive Control1 Intervention

Topical administration to forearm

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

University of Puerto RicoOTHER

62 Previous Clinical Trials

20,788 Total Patients Enrolled

Glyciome, LLCLead Sponsor

Brigham and Women's HospitalOTHER

1,615 Previous Clinical Trials

11,470,788 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many participants are engaging in this clinical experiment?

"Affirmative. Data hosted on clinicaltrials.gov attests to the ongoing recruitment process for this medical trial, which was initially posted on February 24th 2022. 42 patients are needed from a single location."

Answered by AI

Are individuals currently invited to partake in this investigation?

"Affirmative. According to records hosted on clinicaltrials.gov, this medical investigation is actively seeking participants and was first listed on February 24th 2022. The study requires 42 patients from one location; the last revision happened on September 26th of that same year."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Perception & Acceptability of a Cervical Cancer Prevention Prebiotic Device

2022. "Perception & Acceptability of a Cervical Cancer Prevention Prebiotic Device". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04841629.