Other Clinical Trial - High-flow Nasal Cannula Oxygen Therapy With or

See also
Status	Clinical Trial	Phase
Completed	`NCT02105298` - Effect of Volume and Type of Fluid on Postoperative Incidence of Respiratory Complications and Outcome (CRC-Study)	N/A
Active, not recruiting	`NCT04079829` - Postoperative Respiratory Abnormalities
Recruiting	`NCT01857674` - Evaluation of Laryngeal Ultrasonography Performance in Predicting Major Post Extubation Laryngeal Edema in Intensive Care Patients	N/A
Recruiting	`NCT01726140` - CPAP Reduces Hypoxemia After Cardiac Surgery	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT02105298 - Effect of Volume and Type of Fluid on Postoperative Incidence of Respiratory Complications and Outcome (CRC-Study)

N/A

Active, not recruiting

NCT04079829 - Postoperative Respiratory Abnormalities

Recruiting

NCT01857674 - Evaluation of Laryngeal Ultrasonography Performance in Predicting Major Post Extubation Laryngeal Edema in Intensive Care Patients

N/A

Recruiting

NCT01726140 - CPAP Reduces Hypoxemia After Cardiac Surgery

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03121482
Study type	Interventional
Source	Poitiers University Hospital
Contact
Status	Completed
Phase	N/A
Start date	April 20, 2017
Completion date	April 17, 2018

High-flow Nasal Cannula Oxygen Therapy With or Without NIV During the Weaning Period — HIGH-WEAN

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms