Autopsy report · NCT03067558

Acute Respiratory Infection Diagnostic Aids (ARIDA) Controlled Accuracy Evaluation Protocol

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Device incorrect colour-coded classification of fast breathing for RR”

The sponsor’s own words in the registry.

Life of this trial

Registered 1 month before it started.
Ran for about 2 months before it stopped.
150 participants enrolled.
No results are posted on the registry.

Vital statistics

Status: Terminated
Sponsor: Malaria Consortium
Sponsor type: University, hospital or other
Conditions: Pneumonia Childhood
Interventions: Children's automated respiratory rate monitor; MK2 Acute Respiratory Infection (ARI) Timer
Participants: 150
Sites: 1
Countries: Ethiopia

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.