Early Mobilization: Evaluation of Feasibility & Security in Pediatric

See also
	Status	Clinical Trial	Phase
	Withdrawn	`NCT03884400` - Distribution of Biospecimens From Biorepositories/Biobanks for Research Use

See also

Status

Clinical Trial

Phase

Withdrawn

NCT03884400 - Distribution of Biospecimens From Biorepositories/Biobanks for Research Use

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	NCT02958124
Study type	Observational
Source	Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact	Damien Moerman
Phone	003227642719
Email	damien.moerman@uclouvain.be
Status	Recruiting
Phase	N/A
Start date	September 2016

Early Mobilization: Evaluation of Feasibility and Security in Pediatric Intensive Care Unit

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms