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Showing 25–39 of 15 matching trials from the live ClinicalTrials.gov search.

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Filters: Condition: Postoperative Respiratory Failure Clear all

Conditions: Pain
Interventions: Not listed
Lead sponsor: Children's Hospital Medical Center, Cincinnati; Other
Eligibility: 6 Years to 17 Years
Enrollment: 1,000 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2010 – 2017
U.S. locations: 15
States / cities: Los Angeles, California • Palo Alto, California • Denver, Colorado + 12 more

Conditions: Ventilatory Depression, Postoperative Respiratory Failure
Interventions: Oxygen Gas for Inhalation; Other
Lead sponsor: Stanford University; Other
Eligibility: 18 Years to 70 Years
Enrollment: 60 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2022 – 2026
U.S. locations: 1
States / cities: Stanford, California

Conditions: Respiratory Depression
Interventions: Capnography monitoring; Device
Lead sponsor: Wake Forest University Health Sciences; Other
Eligibility: 18 Years to 50 Years · Female only
Enrollment: 3 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2015
U.S. locations: 1
States / cities: Winston-Salem, North Carolina

Conditions: Heart Attack, Cardiac Arrest, Congestive Heart Failure, Atrial Fibrillation, Angina, Deep Vein Thrombosis, Pulmonary Embolism, Respiratory Arrest, Respiratory Failure, Pneumonia, Gastrointestinal Bleed, Stomach Ulcer, Delirium, Stroke, Nerve Injury, Surgical Wound Infection
Interventions: Not listed
Lead sponsor: Washington University School of Medicine; Other
Eligibility: 18 Years and older
Enrollment: 73,952 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2012 – 2020
U.S. locations: 1
States / cities: St Louis, Missouri

Conditions: Respiratory Failure, Respiratory Arrest, Respiratory Distress Syndrome, Acute Respiratory Failure, Acute Respiratory Failure With Hypoxia, Acute Respiratory Failure With Hypercapnia, Acute Respiratory Failure Post Surgical, Acute Respiratory Failure Postprocedural, Acute Respiratory Failure Following Trauma and Surgery, Acute Respiratory Failure Requiring Reintubation, Acute Respiratory Failure Post Traumatic, Acute Respiratory Decompensation, Shock, Shock, Septic, Shock, Cardiogenic, Acute Cardiac Failure, Multi Organ Failure, Acute Kidney Failure
Interventions: Observational retrospective cohort to describe data validity; and Data reliability; and Completeness of the data; Other
Lead sponsor: Efficacy Care R&D Ltd; Industry
Eligibility: 18 Years to 90 Years
Enrollment: 50,000 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2019 – 2020
U.S. locations: 1
States / cities: Houston, Texas

Conditions: Respiratory Failure, Respiratory Infection, Aspiration Pneumonia, Pneumonitis, Atelectasis, Bronchospasm
Interventions: Neuromuscular Blocking Agents, Anesthetic Adjuncts; Drug
Lead sponsor: Beth Israel Deaconess Medical Center; Other
Eligibility: 18 Years and older
Enrollment: 3 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2019 – 2022
U.S. locations: 2
States / cities: Boston, Massachusetts

Conditions: Surgery, Anaesthesia, Ventilator-Induced Lung Injury, Lung Injury, Pneumonia, Pneumothorax, Respiratory Distress Syndrome, Adult, Respiratory Insufficiency
Interventions: Not listed
Lead sponsor: European Society of Anaesthesiology; Other
Eligibility: 18 Years and older
Enrollment: 10,690 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2013
U.S. locations: 3
States / cities: Aurora, Colorado • Boston, Massachusetts • Rochester, Minnesota

Conditions: Postoperative Complications
Interventions: Alaris ETCO2 monitor - cont. resp. rate, & apnea events; Device
Lead sponsor: Texas Health Resources; Other
Eligibility: 18 Years and older
Enrollment: 60 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2006 – 2007
U.S. locations: 1
States / cities: Dallas, Texas

Conditions: Respiratory Depression
Interventions: Capnostream; Device
Lead sponsor: Stanford University; Other
Eligibility: 18 Years to 45 Years · Female only
Enrollment: 80 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2015 – 2016
U.S. locations: 1
States / cities: Palo Alto, California

Conditions: Postoperative Atelectasis, Postoperative Hypoxemia, Postoperative Pneumonia, Postoperative Pulmonary Complications, Patient Adherence, Incentive Spirometry, Respiratory Therapy, Respiratory Insufficiency
Interventions: Alarms; Device
Lead sponsor: University of Colorado, Denver; Other
Eligibility: 18 Years to 100 Years
Enrollment: 240 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024
U.S. locations: 1
States / cities: Aurora, Colorado

Conditions: Adolescent Idiopathic Scoliosis, Respiratory Depression, Postoperative Pain
Interventions: pharmacokinetic simulation; Other
Lead sponsor: University of Florida; Other
Eligibility: 10 Years to 18 Years
Enrollment: 14 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2015 – 2017
U.S. locations: 1
States / cities: Gainesville, Florida

Conditions: Tonsillitis, Airway Obstruction, Difficulty Swallowing
Interventions: IV acetaminophen, PO acetaminophen; Drug
Lead sponsor: Kaveh Aslani, MD; Other
Eligibility: 5 Years to 13 Years
Enrollment: 41 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2012 – 2015
U.S. locations: 1
States / cities: Royal Oak, Michigan

Conditions: Respiratory Failure, Acute Respiratory Failure Requiring Reintubation, Pulmonary Edema, Pneumonia, Hypoxia, Acute Kidney Injury
Interventions: Not listed
Lead sponsor: Massachusetts General Hospital; Other
Eligibility: 18 Years and older
Enrollment: 104,000 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2013 – 2014
U.S. locations: 1
States / cities: Boston, Massachusetts

Conditions: Obstructive Sleep Apnea
Interventions: uvulopalatopharyngoplasty with or without sutures; Procedure
Lead sponsor: Virginia Commonwealth University; Other
Eligibility: 21 Years and older
Enrollment: 16 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2004 – 2008
U.S. locations: 1
States / cities: Richmond, Virginia

Conditions: Postoperative Pain
Interventions: Not listed
Lead sponsor: Senthil Sadhasivam; Other
Eligibility: 3 Years to 15 Years
Enrollment: 1,200 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2022 – 2026
U.S. locations: 1
States / cities: Pittsburgh, Pennsylvania

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Multicenter Perioperative Opioid Pharmacogenetic Study

The Effect of Hyperoxia on Ventilation During Recovery From General Anesthesia

OSA Screen Negative With Spinal Duramorph

Systematic Assessment and Targeted Improvement of Services Following Yearlong Surgical Outcomes Surveys

Postoperative Respiratory Abnormalities

Avoiding Neuromuscular Blockers to Reduce Complications

Local Assessment of Ventilatory Management During General Anesthesia for Surgery

Application of Capnography Monitoring on the General Care Nursing Unit

Postoperative Respiratory Monitoring After Neuraxial Opioid Administration for Cesarean Delivery

REMINDers for Incentive Spirometry in PACU (REMIND-IS in PACU)

Anesthetic Optimization in Scoliosis Surgery

Acetaminophen's Efficacy For Post-operative Pain

Effect of Volume and Type of Fluid on Postoperative Incidence of Respiratory Complications and Outcome (CRC-Study)

Study of Effects of Sutures on Results of Palate Surgery for Obstructive Sleep Apnea

Personalizing Perioperative Analgesia in Children