Condition: Vulvovaginal Candidiasis (VVC) · Yeast Vaginitis · Sponsor: Coologics, Inc
The objective of this study is to determine clinical cure rate and safety of a proprietary Vaginal Cooling Device (VCD) in women with VCC. In addition, the safety, mycological cure rates, the speed and efficacy of symptom resolution, vaginal hyphae and polymorphonuclear (PMN) scores, and Quality-of-Life (QoL) parameters will be determined.
This description comes directly from the study's public registry record.
Kimberly J Langdon, MD · 740-206-4287 · kim@coologics.com
Keith Aqua, MD · 561-951-8212 · kaqua@acrcfl.com
Always discuss trial participation with your own doctor first.
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| Pivotal Clinical Research & Associates | Smyrna, Georgia, United States | Recruiting |
| Renew Health Clinical Research | Snellville, Georgia, United States | Recruiting |
| Leavitt Clinical Research | Idaho Falls, Idaho, United States | Suspended |
| Next Innovative Clinical Research | Chicago, Illinois, United States | Recruiting |
| Unified Women's Clinical Research-Raleigh | Raleigh, North Carolina, United States | Recruiting |
| Lyndhurst Clinical Research | Winston-Salem, North Carolina, United States | Recruiting |
| Aviati Health | Memphis, Tennessee, United States | Active Not Recruiting |
| Vilo Research Group, Inc. | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06983041