Patient Guide: Safety and Efficacy of Boric Acid Inserts for Treatment of Vulvovaginal Candidiasis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07109869
Status: 🟢 Enrolling Now
Condition: Vulvovaginal Candidiases, Vulvovaginal Candidiasis, Genital, Vulvovaginal Candidiasis (VVC)
Phase: PHASE3

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Phoenix, Arizona
  • • Huntington Park, California
  • • And 17 more locations

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Safety and Efficacy of Boric Acid Inserts for Treatment of Vulvovaginal Candidiasis - Join Clinical Trial NCTNCT07109869

How to Join This Clinical Trial - NCTNCT07109869

Learn how to participate in this PHASE3 trial studying an investigational therapy for Vulvovaginal Candidiases, Vulvovaginal Candidiasis, Genital, Vulvovaginal Candidiasis (VVC). This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Vulvovaginal Candidiases, Vulvovaginal Candidiasis, Genital, Vulvovaginal Candidiasis (VVC). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Vulvovaginal Candidiases, Vulvovaginal Candidiasis, Genital, Vulvovaginal Candidiasis (VVC)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT07109869 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 20 locations. Find a study site near you:

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85031 - United States

Status: RECRUITING

Clinical Research Site

Huntington Park, California 90255 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90057 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33125 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33176 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33184 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33607 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33634 - United States

Status: RECRUITING

Clinical Research Site

Idaho Falls, Idaho 83404 - United States

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Vulvovaginal Candidiases, Vulvovaginal Candidiasis, Genital, Vulvovaginal Candidiasis (VVC):

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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