Autopsy report · NCT03647462
Impact of Early Diagnosis and Treatment of OSA on Hospital Readmission in Hospitalized COPD Patients
Cause of deathOther, also slow enrollment
“The study was withdrawn prior to initiation. The protocol was submitted for IRB review but was not approved. No participants were enrolled.”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- Kaiser Permanente
- Sponsor type
- University, hospital or other
- Conditions
- Obstructive Sleep Apnea; Chronic Obstructive Pulmonary Disease
- Interventions
- Continuous Positive Airway Pressure
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- CPAP Population Management
“The study was withdrawn prior to initiation. The protocol was submitted for IRB review but was not approved, and no participants were enrolled.” - Antibiotics and Tissue Expanders in Breast Reconstruction
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“Study never initiated; withdrawn prior to receiving IRB approval” - RCT Investigating Pre-cesarean Vaginal Wash of Chlorhexidine vs Povidone-iodine for Patient With Ruptured Amniotic Membrane.
“The study was withdrawn from the IRB” - Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
“Study did not receive IRB approval, so did not start”
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.