Autopsy report · NCT06742229

Clinical Data Collection for Obstetric Ultrasound Algorithms

“Study paused temporarily pending IRB approval of an amendment to the protocol and consent form.”

The sponsor’s own words in the registry.

Life of this trial

• Suspended: paused, and may or may not restart.
• 700 participants planned (an estimate, not an actual count).

Vital statistics

Status

Suspended

Phase

Na

Sponsor

Caption Health, Inc.

Sponsor type

Industry

Conditions

Pregnancy

Interventions

Research Ultrasound scan

Participants

700 (planned, not actual)

Sites

3

Countries

United States

Trials that died the same way

• Simvastatin Nasal Rinses for the Treatment of COVID-19 Mediated Dysomsia
  “Study halted prematurely; IRB approval not obtained” (80% match in meaning)
• Exhaled Breath Condensate pH in Patients With Cough Caused by Gastroesophageal Reflux
  “IRB approval not renewed/approval lapsed. Prior status: insufficient enrollment; study suspended pending analysis” (79% match in meaning)
• Risk Screening & Primary Prevention of Elder Abuse in People Living With Dementia
  “Study paused per IRB request.” (79% match in meaning)
• Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
  “Study never initiated; withdrawn prior to receiving IRB approval” (77% match in meaning)
• Bortezomib in Combination With Ibrutinib in Ibrutinib Relapsed Mantle Cell Lymphoma
  “Enrollment and/or interactions/interventions temporarily paused due to COVID-19 and expected to resume in the future. This is not a suspension of IRB approval.” (76% 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.