Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00875134
Other study ID # 10-06-54
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date March 2009
Est. completion date March 2010

Study information

Verified date June 2019
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to test the ability of a computer-based algorithm to detect and intervene in cases of narcotic-induced respiratory depression.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 2010
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Elective surgical patients

Exclusion Criteria:

- Refusal to consent to study

Study Design


Intervention

Other:
Verbal prompt
Patient hears a voice recording
Skin Stimulus
Patient receives either a skin stimulus

Locations

Country Name City State
United States Oregon Health and Science University Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy in treating respiratory depression seconds after desaturation
See also
  Status Clinical Trial Phase
Active, not recruiting NCT03441282 - Precision Medicine in Anesthesia: Genetic Component in Opioid-induced Respiratory Depression
Completed NCT02907255 - Vital Sign Monitoring With Continuous Pulse Oximetry and Wireless Clinician Notification After Surgery N/A
Completed NCT00544947 - Observation of Respiration Following Regional Anaesthesia With Intrathecal Opioids for Caesarean Section N/A
Completed NCT02987985 - Efficacy of Opioid-free Anesthesia in Reducing Postoperative Respiratory Depression in Children Undergoing Tonsillectomy Phase 3
Recruiting NCT05391555 - Pupillary Unrest as an Indicator of Central Opioid Effect in Subjects 40-60 Years of Age Phase 2/Phase 3
Completed NCT02481570 - Anesthetic Optimization in Scoliosis Surgery N/A
Completed NCT06083272 - VitalThings Guardian Contactless Monitoring
Not yet recruiting NCT06064409 - Optimal Timing and Failure Prediction of High Flow Nasal Cannula Oxygen Therapy in Emergency Department: Prospective Observational Single Center Study
Completed NCT00345384 - Dexmedetomidine for the Control of Post-Operative Pain in Thoracotomy Patients Phase 1/Phase 2
Recruiting NCT04046068 - Multimodal Perioperative Pain Management: ComfortSafe Program
Recruiting NCT02819661 - Respiratory Depression in Women With BMI≥30 Underwent Spinal Anesthesia With Intrathecal Morphine in Elective C-section N/A
Active, not recruiting NCT04011163 - Vital Signs-Integrated Patient-Assisted Intravenous Opioid Analgesia for Post Surgical Pain Phase 2/Phase 3
Active, not recruiting NCT06374589 - Closed-Loop O2 Use During High Flow Oxygen Treatment Of Critical Care Adult Patients (CLOUDHFOT) N/A
Terminated NCT02760927 - Assessment of a Oral Endotracheal Tube Fastener on Patients Intubated With Oral Endotracheal Tubes N/A
Completed NCT01869582 - Safer Births - Reducing Perinatal Mortality N/A
Not yet recruiting NCT06137638 - ENA-001 for Post Operative Respiratory Depression (PORD) Phase 2
Completed NCT01843933 - Detecting Post-Operative Respiratory Depression in Children N/A
Completed NCT00696137 - Long-term Extension Study of BEMA™ Fentanyl Phase 3
Completed NCT04017702 - Detection of Postoperative Respiratory Depression in High Risk Patients Utilizing Minute Ventilation Monitoring
Withdrawn NCT04495452 - Precision Medicine in Anesthesia