Other Clinical Trial - Evaluation of the Lung Recruitment & End-expiratory

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Acute Lung Injury
ARDS: Acute Respiratory Distress Syndrome
Pulmonary Atelectasis
Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Newborn
Syndrome

See also
	Status	Clinical Trial	Phase
	Completed	`NCT05933291` - Single-cell Landscape of BALF in Patients With Severe ARDS and CARDS
	Enrolling by invitation	`NCT06117761` - Combined Activity and Cognitive Intervention for ICU Survivors	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT05933291 - Single-cell Landscape of BALF in Patients With Severe ARDS and CARDS

Enrolling by invitation

NCT06117761 - Combined Activity and Cognitive Intervention for ICU Survivors

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	NCT01670747
Study type	Observational
Source	Policlinico Hospital
Contact
Status	Completed
Phase	N/A
Start date	September 2012
Completion date	March 2015

Evaluation of the Lung Recruitment and End-expiratory Lung Collapse in Acute Respiratory Distress Syndrome (ARDS)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms