Autopsy report · NCT01516697
Non-invasive Cardiac Output Monitoring in Obstetric Patients
Cause of deathStaffing, sites or logistics, also slow enrollment
“unable to enrollment subjects due to early departure of study personele”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Phase 4
- Sponsor
- Massachusetts General Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Complications; Cesarean Section; Anesthesia; Adverse Effect, Spinal and Epidural
- Interventions
- experimental; Control
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- A Study of CCCTC-binding Factor (CTCF) in Infantile Hemangiomas
“no subjects were enrolled, study was halted due to study staff departure” - Treatment of Chronic Post-Traumatic Headache With OnabotulinumtoxinA
“Study discontinued due to difficulty in enrolling eligible subjects” - The Impact of Salmeterol-Fluticasone on Sleep in Patients With COPD
“Study subject enrollment difficulties” - Inferior Vena Cava (IVC) Diameters Before & After Interscalene Block
“unable to enroll subjects” - Efficacy Study of Altabax to Clear Methicillin-resistant Staphylococcus Aureus (MRSA) Nasal Colonization
“Study is withdrawn and no one enrolled due to changes in personnel”
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.