Autopsy report · NCT01930877
Effect of Perioperative Intravenous Lidocaine on Postoperative Quality of Recovery in Patients Undergoing Spine Surgery
Cause of deathStaffing, sites or logistics
“Withdrawn by PI”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 2
- Sponsor
- Baylor College of Medicine
- Sponsor type
- University, hospital or other
- Conditions
- Pain
- Interventions
- Lidocaine; Placebo (normal saline)
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Histidine Oral Supplementation as a Therapeutic Modality for Alzheimer's Disease
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“PI withdrawn” - EXCOR® Pediatric VAD Anticoagulation IDE
“PI withdrew protocol” - Conventionally vs. Digitally Fabricated Complete Dentures: Clinical Treatment Outcome Differences
“The PI is deceased, decision was made to withdraw.” - Mechanical Ventilation in Severe Brain Injury: The Effect of Positive End Expiratory Pressure on Intracranial Pressure
“Departure of PI”
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.