Autopsy report · NCT07038512
Evaluation of Hyivy Floora in Managing Interstitial Cystitis/Bladder Pain Syndrome/High-tone Pelvic Floor Dysfunction
Cause of deathDrug or device supply
“Study has been withdrawn due to ongoing difficulties with device manufacturing and our inability to reach the sponsor team for updates or guidance over the recent period.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Na
- Sponsor
- Wake Forest University Health Sciences
- Sponsor type
- University, hospital or other
- Conditions
- Interstitial Cystitis/Painful Bladder Syndrome; Interstitial Cystitis, Chronic; High Tone Pelvic Floor Dysfunction
- Interventions
- Floora Pelvic Rehabilitation Vaginal Dilator
- Participants
- 0
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“Study was withdrawn due to scientific and business considerations.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.