Autopsy report · NCT03461666

Comparison of Efficacy of Behavioral Approaches for Treatment of Insomnia

“Study halted prematurely and will not resume; participants are no longer being examined or receiving intervention. COVID Complications.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 8 months before it started.
• Ran for about 3 years 10 months before it stopped.
• 160 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Pacific Institute of Medical Sciences

Sponsor type

University, hospital or other

Conditions

Primary Insomnia

Interventions

Cognitive Behavior Therapy-Insomnia; Focus of Attention; Combined-CBT-I and FOA Group; Sleep Hygiene

Participants

160

Sites

2

Countries

United States

Trials that died the same way

• Secukinumab for NLD (Cosentyx) in Patients With Necrobiosis Lipoidica Diabeticorum (NLD)
  “Study halted prematurely due COVID-19 pandemic and did not resume; participants are no longer being examined or receiving intervention.” (93% match in meaning)
• New Formulations of Propafenone to Treat Atrial Fibrillation
  “Study halted/terminated prematurely due to COVID.” (87% match in meaning)
• Perception-Action Approach vs. Passive Stretching for Infants With Congenital Muscular Torticollis
  “Study stopped due to COVID-19 pandemic and will not resume.” (84% match in meaning)
• Zambia Common Elements Treatment Approach Pilot Study
  “COVID-19 precluded the study team from being able to complete all follow-up assessments.The study was halted on March 17, 2020 and did not resume.” (82% match in meaning)
• FMT for MDRO Colonization After Infection in Renal Transplant Recipients
  “This study was paused and was not resumed due to the COVID-19 pandemic.” (81% 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.