Autopsy report · NCT03938532

Feasibility and Impact of Volume Targeted Ventilation in the Delivery Room

“Discontinuation of the study Product by manufacturer”

The sponsor’s own words in the registry.

Life of this trial

• Registered 3 months before it started.
• Ran for about 5 years 6 months before it stopped.
• 20 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Baystate Medical Center

Sponsor type

University, hospital or other

Conditions

Prematurity; BPD - Bronchopulmonary Dysplasia; Respiratory Distress Syndrome, Newborn

Interventions

Volume Targeted Ventilation (VTV) using the Philips Respironics NM3 monitor; Tidal Volume Measurement using the Philips Respironics NM3 monitor

Participants

20

Sites

1

Countries

United States

Trials that died the same way

• Safety and Efficacy of Ustekinumab in Patients With Palmo-Plantar Pustular Psoriasis or With Palmo-Plantar Pustulosis
  “Manufacturer ceased to produce vials used for this study.” (69% match in meaning)
• Nanoparticles and Hypofractionated Protontherapy for Reirradiation of Pantumor Relapse
  “Study prematurely terminated following the decision by industrial partner to withdraw from the project (product supply issue).” (68% match in meaning)
• SHR-1210 in Combination With BP102 and XELOX in Patient With Metastatic Colorectal Cancer
  “The study was terminated early due to company decision” (66% match in meaning)
• Cannabinoids in PLWHIV on Effective ART
  “expiration of study product; end of study product availability” (66% match in meaning)
• Study to Investigate Comparative Efficacy, Safety and Immunogenicity Between AVT16 and Entyvio
  “The study has been terminated based on Sponsor decision. This decision is not related to any safety concerns associated with the investigational products. It is related to the fact that study will be not required for product dossier submission.” (66% 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.