Effect Of Clustered Nursing Interventions On Physiological Response In Critically Ill Patients
NCT ID: NCT04134481
Last Updated: 2019-10-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
80 participants
OBSERVATIONAL
2015-09-15
2017-04-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Nursing Care for Breathing Discomfort Among Mechanically Ventilated Patients
NCT04019236
Mechanical Ventilation Practices in Uganda's Intensive Care Units
NCT03800849
Looking at the Physiological Response of Ergometry in Critical Care Patients
NCT04383171
Respiratory Mechanics in Intensive Care Patients
NCT03420417
The Effectiveness of the Modified Bundle in the Prevention of VAP.
NCT04038814
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
low intervention group
from 0-7 clustered nursing intervention
No interventions assigned to this group
high intervention group
from 8-15 clustered nursing intervention
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* mechanically ventilated for ≥ 48 hours.
Exclusion Criteria
* pregnancy.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Alexandria University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Amr Hassan Dahroug
lecturer, critical care medicine
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
amr dahroug
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.