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Comparison effect of two implemented sedation methods (Scale & protocol) by nurses on some consequences of mechanical ventilation in intensive care patients

Comparison effect of two implemented sedation methods (Scale & protocol) by nurses on some consequences of mechanical ventilation in intensive care patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201098665N1
Enrollment
25
Registered
2012-07-04
Start date
2012-06-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: pneumonia due to mechanical ventilation. Condition 2: mechanical ventilation duration. Condition 3: intra tracheal tube duration. Condition 4: time each of mechanical ventilation mode. Pneumonia, organism unspecified Respiratory conditions due to unspecified external agent Other specified misadventures during surgical and medical care Other specified medical care

Interventions

Intervention 1: after finishing control group sampling, randomly in one section of ICU ward of Alzahra Hospital of Isfahan implement scale and in another part protocol. it is noticeable that selection
Treatment - Drugs
after finishing control group sampling, randomly in one section of ICU ward of Alzahra Hospital of Isfahan implement scale and in another part protocol. it is noticeable that selection of patients are
at first for determination of routine method effect on outcomes of mechanical ventilation, patients who have inclusion criteria are selected as samples and is done parameteres. at current ways that is
In protocol group, at first agitation score of each patient measured by nurse, and if Richmond score of patient was more than zero, ventilators and other devices are assessed by nurse, and after corre

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: age above18y and under 65y; under mechanical ventilation with Positive pressure; attachment to mechanical ventilation more than 48h; need to sedative drugs in treatment plan. exclusion criteria: Tracheostomy; weaning before 24h; using neuromuscular blocker drugs; after CPR; severe hearing loss; pripheral nervous system disorders; addiction; pneumonia before 48h of attchment to mechanical ventilation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical pneumonia due to mechanical ventilation. Timepoint: first and fourth day of admission. Method of measurement: physician diagnosis.

Secondary

MeasureTime frame
Mechanical ventilation duration. Timepoint: hour. Method of measurement: from attchment to ventilator until weaning time.;Hospitalization time in ICU. Timepoint: hour. Method of measurement: from admission in ICU until discharge time.;Intra tracheal tube duration. Timepoint: hour. Method of measurement: from insertion tracheal tube until exiting.;Mechanical ventilation modes. Timepoint: hour. Method of measurement: including Spont, SIMV, Bilevel.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabamohamadi, Hassan

Semnan University of Medical Sciences

babamohamadi@sem-ums.ac.ir+98 23 1335 4190

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026