Autopsy report · NCT00768742
Safety and Effectiveness Study of RF Ablation of Uterine Fibroids to Reduce Menstrual Bleeding: the Fibroid Ablation Study
Cause of deathOther
“study revised and reinitiated under another protocol”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Gynesonics
- Sponsor type
- Industry
- Conditions
- Leiomyoma; Uterine Fibroids; Menorrhagia
- Interventions
- VizAblate Intrauterine Ultrasound-Guided RF Ablation
- Participants
- 0
- Sites
- 3
- Countries
- Canada
Trials that died the same way
- Estimate Serum Oxytocin PD Range in the Periphery
“Study will be replaced by a revised study protocol” - Immunotherapy With N 803, ETBX-071, and M-CENK in Combination With Radiation for Participants With High-Risk Prostate Cancer.
“Study was redeveloped into a new protocol” - Nitric Oxide During Cardiopulmonary Bypass in Neonates to Reduce Risk of Acute Kidney Injury
“revised and combined with another protocol” - Effect of HAART Vs. Statin Treatment on Endothelial Function and Inflammation/Coagulation
“On 05/08/12, team working on revising protocol and re-open study under version 2.0” - Study of Stored Tumor Samples in Young Patients With Brain Tumors
“New Protocol that replaces the current study”
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.