PRediction of Opioid-induced Respiratory Depression In Patients Monitored by capnoGraphY

NACompletedINTERVENTIONAL
Enrollment

1,495

Participants

Timeline

Start Date

April 7, 2017

Primary Completion Date

May 7, 2018

Study Completion Date

May 7, 2018

Conditions
Respiratory Depression
Interventions
DEVICE

Capnostream Monitor

Capnography and pulse oximetry monitoring data will be collected for up to 48 hours while patients are on the hospital ward. In addition, a 1-month follow up will be completed.

Trial Locations (16)

14203

Buffalo General Medical Center, Buffalo

30322

Emory University Hospital, Atlanta

43210

The Ohio State University Wexner Medical Center, Columbus

44109

MetroHealth Medical Center, Cleveland

44195

Cleveland Clinic, Cleveland

46010

Hospital Clínico Universitario de Valencia, Valencia

48073

Beaumont Hospital - Royal Oak, Royal Oak

53127

University Hospital Bonn, Bonn

80045

University of Colorado Hospital, Aurora

92151

Hospital Foch, Suresnes

119074

National University Hospital, Singapore

02115

Brigham and Women's Hospital, Boston

98201-1689

Providence Regional Medical Center Everett, Everett

700-8558

Okayama University Hospital, Okayama

105-8471

The Jikei University School of Medicine Hospital, Tokyo

6229 HX

Maastricht UMC+, Maastricht

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Medtronic - MITG

INDUSTRY