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NCT04134481 Clinical Trial

Effect Of Clustered Nursing Interventions On Physiological Response In Critically Ill Patients

Mechanically Ventilated Patients Clinical Trial

Official title:
Physiological Responses Related to Clustered Nursing Interventions Among Mechanically Ventilated Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04134481
Other study ID # amr dahroug
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 15, 2015
Est. completion date April 1, 2017

Study information
Verified date October 2019
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To determine physiological responses related to clustered nursing interventions among critically ill patients.

Description:

Clustered nursing interventions are defined as group of interventions more than six for each patient in one nursing interaction.The study was conducted on 80 mechanically ventilated adult patients admitted to intensive care units of Alexandria Main University Hospital and Damanhour Medical National Institute. The most common procedures provided by nurses in direct care for those patients were vital signs measurements, central venous pressure measurement, suctioning, feeding, laboratory sampling, general care, repositioning, and administration of medications. Physiological parameters measured were end-tidal carbon dioxide using capnography, vital signs using bed side monitor, and oxygen saturation using pulse oximeter.

Recruitment information / eligibility
Status Completed
Enrollment 80
Est. completion date April 1, 2017
Est. primary completion date April 1, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- adult patients of both sex, aged 18 years and over

- mechanically ventilated for = 48 hours.

Exclusion Criteria:

- lung disorder (eg, COPD, asthma, lung cancer, pneumonia, ARDS)

- pregnancy.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Alexandria University

Outcome
Type Measure Description Time frame Safety issue
Primary change in end tidal CO2 in mmHg (EtCO2) change in oxygen saturation (SO2) measured 5 min before procedure (baseline), 5 min after start, 10 min after, immediately at end procedure, 15 min after end procedure for two weeks up to 14 days
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