Autopsy report · NCT06698185

A Clinical Phase II Study of the Materna Device to Shorten Delivery Time During Childbirth

“Change in IRB jurisdiction for study, study is suspended”

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• Withdrawn before it enrolled anyone.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Withdrawn

Phase

Na

Sponsor

Materna Medical

Sponsor type

Industry

Conditions

Childbirth

Interventions

Materna Prep Device; Sham Control

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• A Pragmatic Randomized Trial of Icosapent Ethyl for High-Cardiovascular Risk Adults
  “The study was suspended by the IRB of record and subsequently terminated” (75% match in meaning)
• Reducing Frailty for Older Cancer Survivors Using Supplements II
  “The study has been suspended by the IRB pending review of a study-related issue” (73% match in meaning)
• A Quality of Life Study Using Insulin Potentiation Targeted LowDose (IPTLD) Chemotherapy and Nutrition Therapy in the Treatment of Cancer
  “The IRB which was overseeing the study stopped overseeing it” (71% match in meaning)
• RCT Investigating Pre-cesarean Vaginal Wash of Chlorhexidine vs Povidone-iodine for Patient With Ruptured Amniotic Membrane.
  “The study was withdrawn from the IRB” (69% match in meaning)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” (69% 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.