Looking at the Physiological Response of Ergometry in Critical Care

Clinical Trial Description

This study explores the physiological and metabolic demands of passive ergometry as a step in active rehabilitation and compares two methods of monitoring these changes in critically ill patients. ;

Study Design

Related Conditions & MeSH terms

Critical Ill Patients

See also
	Status	Clinical Trial	Phase
	Completed	`NCT03176329` - Closed-loop Versus Conventional Ventilation Mode During Mobilization Period in Critical Care Patients	N/A
	Completed	`NCT02355873` - Efficacy and Safety of Heparin-coated Surface-treated Polyacrylonitrile Membrane Hemofilter in Critical Ill CRRT Patients	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT03176329 - Closed-loop Versus Conventional Ventilation Mode During Mobilization Period in Critical Care Patients

N/A

Completed

NCT02355873 - Efficacy and Safety of Heparin-coated Surface-treated Polyacrylonitrile Membrane Hemofilter in Critical Ill CRRT Patients

Phase 4

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	NCT04383171
Study type	Observational
Source	University Hospital Southampton NHS Foundation Trust
Contact
Status	Completed
Phase
Start date	March 17, 2015
Completion date	June 7, 2017

Looking at the Physiological Response of Ergometry in Critical Care Patients

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms