Other Clinical Trial - The Efficacy & the Safety of Dexmedetomidine

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Failed Conscious Sedation During Procedure

See also
Status	Clinical Trial	Phase
Terminated	`NCT03401606` - Controlled Sedation for Cataract Surgery	Phase 4
Completed	`NCT02121704` - Magnetic Endoscope Imaging in Colonoscopy: Influence on Propofol Dosage	N/A
Recruiting	`NCT01390675` - Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

See also

Status

Clinical Trial

Phase

Terminated

NCT03401606 - Controlled Sedation for Cataract Surgery

Phase 4

Completed

NCT02121704 - Magnetic Endoscope Imaging in Colonoscopy: Influence on Propofol Dosage

N/A

Recruiting

NCT01390675 - Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

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	NCT02296073
Study type	Interventional
Source	Anhui Provincial Children's Hospital
Contact
Status	Not yet recruiting
Phase	Phase 4
Start date	December 2014
Completion date	December 2015

The Efficacy and the Safety of Dexmedetomidine Sedation on the Pediatric Intensive Unit(PICU) Patients.

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms