Autopsy report · NCT00278434
Zoledronate in Treating Patients With Cervical Intraepithelial Neoplasia 2/3 or 3
Cause of deathSlow enrollment
“Accrual was insufficient to meet study endpoints”
Life of this trial
- Registered 9 months after it had already started.
- Ran for about 3 years 3 months before it stopped.
- 12 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- University of California, San Francisco
- Sponsor type
- University, hospital or other
- Conditions
- Cervical Cancer; Precancerous Condition
- Interventions
- Zoledronate; Placebo (Saline)
- Participants
- 12
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Obstruction of Malignancy: Percutaneous Renal vs Endoscopic Stent
“Study stopped due to lack of accrual” - Evaluation of 3TC or FTC Mono-therapy Compared to Continuing HAART as a Bridging Strategy
“Study was halted for lack of accrual” - Observation of Outcomes and Side Effects of Cesium-131 in Combination With External Beam Radiation for the Treatment of Intermediate to High Risk Prostate Cancer
“Study never moved forward due to no accrual” - High Dose Rate Brachyablation of Primary Liver Lesions
“Study was closed due to poor accrual” - Dehydroepiandrosterone (DHEA) and Letrozole in Treating Patients With Metastatic Breast Cancer
“Study was terminated due to lack of accrual”
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.