JPRN-UMIN000026993
Completed
未知
PRediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphY (PRODIGY) - PRODIGY
ConditionsPatients monitored by capnoGraphY
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Patients monitored by capnoGraphY
- Sponsor
- Covidien Japan Inc.
- Enrollment
- 1650
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\.Expected length of stay \=\<24 hours. 2\.Patient is receiving intrathecal opioids. 3\.Post\-surgical patients with American Society of Anesthesiologists physical status (ASA PS) V or higher. 4\.Patients with the status of Do Not Resuscitate (DNR), hospice, or receiving end of life therapy. 5\.Ventilated or intubated patients. 6\.Patient is unwilling or unable to comply fully with study procedures (including non\-toleration of the capnography cannula) due to any disease condition which can raise doubt about compliance and influencing the study outcome. 7\.Patient is a member of a vulnerable population, includinglegal incapacity or evidence that a subject cannot understand the purpose and risks of the study, regardless of authorized representative support. 8\.Patient is participating in another potentially confounding drug or device clinical study.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
PRediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphYopoid induced RDrespiratory depression10038716NL-OMON42863Medtronic B.V.330
Active, not recruiting
Phase 1
Treatment of respiratory depression from opioids in healthy volunteers and opioid usersEUCTR2021-005373-51-NLeiden University Medical Center24
Recruiting
Phase 4
Reversal of opioid-induced respiratory depression with opioid antagonists - a study in opioid naïve individuals and chronic opioid users under real-life conditionsPK en PD (farmacokinetiek en farmacodynamiek)opioid-induced respiratory depressionNL-OMON54257eids Universitair Medisch Centrum24
Active, not recruiting
Phase 1
Reversal of opioid-induced respiratory depression by ketamine in healthy volunteersRespiratory depressionMedDRA version: 19.0Level: LLTClassification code 10069144Term: Acute respiratory insufficiencySystem Organ Class: 100000004855MedDRA version: 19.0Level: LLTClassification code 10038701Term: Respiratory insufficiencySystem Organ Class: 100000004855Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]EUCTR2016-002148-17-NLMC12
Recruiting
Not Applicable
Reversal of opioid-induced respiratory depression (OIRD) by ketamine in healthy volunteersNL-OMON24921MC12