Autopsy report · NCT01300221

Real-time 3-Dimensional Echocardiography for Assessment of Cardiac Function and Congenital Heart Disease

“Study did not receive IRB approval.”

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• Withdrawn before it enrolled anyone.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Withdrawn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

Drexel University

Sponsor type

University, hospital or other

Conditions

Congenital Heart Disease

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Retroperitoneal Ligation of Uterine Artery in Total Laparoscopic Hysterectomy for Enlarged Uterus
  “IRB did not approve this study.” (89% match in meaning)
• Light Therapy to Treat Depression in Pediatric Stem Cell Therapy Recipients
  “The study did not enroll participants and had not shown significant progress since the initial IRB approval.” (89% match in meaning)
• Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
  “Study never approved by the IRB. Was not initiated” (88% match in meaning)
• Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
  “Study did not receive IRB approval, so did not start” (85% match in meaning)
• Supervisory Neglect, Non-Accidental Trauma, Brief Intervention, and Treatment Referral
  “Study was never initiated. No IRB approval obtained, and no participants enrolled.” (85% 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.