Patient Guide: A Randomised, Partly Blinded Investigation to Evaluate the Clinical Performance and Safety of pHyph in Adult Women With Vulvovaginal Candidiasis Compared With an Untreated Control Group

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✓ Get matched to the right study location for you
✓ Connect directly with study coordinators at 3 participating sites
✓ Understand eligibility with our simplified screening tool
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Trial ID: NCTNCT07405853

Status: NOT_YET_RECRUITING

Condition: Vulvovaginal Candidiasis (VVC)

Phase: NA

Find a Study Location Near You

This study is available at 3 research sites. We'll help you connect with the location that's right for you.

Participating sites include:

• Linköping,
• Solna,
• Uppsala,

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A Randomised, Partly Blinded Investigation to Evaluate the Clinical Performance and Safety of pHyph in Adult Women With Vulvovaginal Candidiasis Compared With an Untreated Control Group - Join Clinical Trial NCTNCT07405853

How to Join This Clinical Trial - NCTNCT07405853

Learn how to participate in this NA trial studying an investigational therapy for Vulvovaginal Candidiasis (VVC). Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with 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 Candidiasis (VVC)
Treatment Being Tested: Investigational treatment
Study Phase: NA - Research study
Enrollment Status: NOT_YET_RECRUITING
Study Identifier: NCTNCT07405853 - 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 3 locations. Find a study site near you:

Clinical Research Site

Linköping, - Sweden

Status: Contact for availability

Clinical Research Site

Solna, - Sweden

Status: Contact for availability

Clinical Research Site

Uppsala, 75237 - Sweden

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Vulvovaginal Candidiasis (VVC):

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

Why Choose Quri.ai as Your Clinical Trial Matching Service

Quri.ai is a free clinical trial matching service that helps patients connect with research sites. We make it easier to:

Find clinical trials that match your condition
Get matched to the right study location near you
Connect directly with study coordinators
Understand if you qualify with simplified eligibility screening
Navigate the enrollment process with personalized support
Access new treatments through clinical research participation