Evaluation of the Efficacy of Oxygen Therapy & Clinical Feasibility of

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05192629` - Intranasal Dexmedetomidine Versus Oral Midazolam as Premedication for Propofol Sedation in Pediatric Patients Undergoing Magnetic Resonance Imaging	Phase 3
Recruiting	`NCT04483258` - Sevoflurane Insufflation vs Intravenous Sedation for Radiotherapy in Pediatric Patients	N/A
Completed	`NCT03956342` - ClinRO Sedation Validation

See also

Status

Clinical Trial

Phase

Recruiting

NCT05192629 - Intranasal Dexmedetomidine Versus Oral Midazolam as Premedication for Propofol Sedation in Pediatric Patients Undergoing Magnetic Resonance Imaging

Phase 3

Recruiting

NCT04483258 - Sevoflurane Insufflation vs Intravenous Sedation for Radiotherapy in Pediatric Patients

N/A

Completed

NCT03956342 - ClinRO Sedation Validation

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	NCT04852432
Study type	Interventional
Source	Seoul National University Hospital
Contact	Jin-Tae Kim, MD, PhD
Phone	02-2072-3661
Email	jintae73@gmail.com
Status	Recruiting
Phase	N/A
Start date	July 27, 2021
Completion date	December 30, 2024

Evaluation of the Efficacy of Oxygen Therapy and Clinical Feasibility of High Flow Nasal Cannula During Moderate and Deep Sedation in Pediatric Patients

Clinical Trial Summary

Clinical Trial Description

Study Design

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