Autopsy report · NCT04807387
Newly Designed Vaginal Stent to Improve Patient Comfort and Healing Following Vaginal Surgery or Vaginal Radiation
Cause of deathFunding or business, also regulatory or ethics
“After enrolling 6 healthy participants the study is being put on halted due to funding and personnel gap. All participants have been informed, per study IRB, of study status.”
Life of this trial
- Registered 1 year 2 months before it started.
- Ran for about 8 months before it stopped.
- 6 participants enrolled.
- Results were posted on the registry 1 year 7 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Baylor College of Medicine
- Sponsor type
- University, hospital or other
- Conditions
- Vaginal Stricture
- Interventions
- Vaginal Stent A; Vaginal Stent B; Vaginal Stent
- Participants
- 6
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Risk Screening & Primary Prevention of Elder Abuse in People Living With Dementia
“Study paused per IRB request.” - Safety and Efficacy Study of Electrotransfer of Plasmid AMEP to Treat Advanced or Metastatic Melanoma
“The study has been halted due to the low enrolment rate.” - Omission of Surgery in Clinically Low-risk HER2positive Breast Cancer With High HER2 Addiction and a Complete Response Following Standard Anti-HER2-based Neoadjuvant Therapy
“The study was prematurely halted primarily due to low patient accrual. Despite efforts to optimize recruitment, the enrollment rate remained insufficient to meet the predefined targets, and continuation was deemed unfeasible” - The Effect of Buprenorphine Continuation for Patients With Opioid Use Disorder
“This study was halted prior to accumulating the full number of participants due to difficulty in recruiting study subjects.” - The Role of Osteopathic Manipulative Medicine in Recovery From Concussions
“Due to lower than anticipated enrollment number, this study was stopped.”
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.