Autopsy report · NCT01094197

Detailed Evaluation of Microchimerism

“Investigators could not identify subjects who met all inclusion criteria.”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Sponsor

Vitalant Research Institute

Sponsor type

University, hospital or other

Conditions

Chimerism; Blood Transfusion; Wounds and Injuries; Hematopoiesis

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• SOM230 Ectopic ACTH-producing Tumors
  “Due to stringent inclusion/exclusion criteria, study investigator deemed it not feasible.” (72% match in meaning)
• Study of Viscosupplementation for the Treatment of Knee Pain After Menisectomy
  “Patients did not meet inclusion criteria.” (71% match in meaning)
• Neoadjuvant Chemotherapy Plus Nephroureterectomy for Locally Advanced Upper Tract Transitional Cell Cancer
  “Study was unable to recruit subjects meeting the study requirements.” (68% match in meaning)
• Gastric and Autonomic Functions in Patients With Intragastric Balloon
  “The study did not recruit any participant.” (68% match in meaning)
• Phrenic Nerve Stimulation for Treatment of Central Sleep Apnea
  “No eligible subjects were identified.” (67% match in meaning)

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.