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Evaluation of pneumonia number, weaning time that help in breathing and stay of hospital time of patients that breath for tracheostomy and used Machine for Help in Cough.

Evaluation of lung infection rates, weaning time and hospital admission time in tracheostomized patients who used the use of an Insufflation- Exsuflation pulmonary mechanism when compared to those who did not use cough assit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6s99yw
Enrollment
Unknown
Registered
2018-10-10
Start date
2015-09-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

pneumonia

Interventions

It is a randomized and prospective clinical study conducted in two groups: G1 (control group): 24 patients tracheostomy in use of mechanical ventilation are follow time of weaning, length of hospital
G2: 24 patients in use of mechanical ventilation will use MI-E application will undergo bronchial hygiene using IM-E, applied with the Coughtassist® CA-3200 Philips / Respironics device, this will be
Procedure/surgery

Sponsors

Hospital de Clinicas da Unicamp
Lead Sponsor
Hospital de Clinicas da Unicamp
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients both male and female; aged 18 years and less or equal to 80 years; admitted to the Intensive Care Unit; tracheostomized; underwent invasive mechanical ventilation with Fio2 <60% and PEEP < 10 cmH2O; hemodynamically stable; subjects who agree to participate in the research must sign a free and informed consent form.

Exclusion criteria

Exclusion criteria: Patients who are not in the 18 to 80 age group will be excluded from the study; Major abdominal distention; Neurologic patients without ICP control (intracranial pressure); Patients with a history of asthma or severe bronchospasm; with a history of osteosporosis, pneumothorax, pneumomediastinum, costal arch fracture, skull base fracture, and cystic fistula; Patients who are not in ventilatory weaning.

Design outcomes

Primary

MeasureTime frame
The aplication of insuflation and exsuflation mechanism do not cause higher or less 20 beats per minute of heart rate, monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause higher or less 20 mercury milimeters of mean blood pressure monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause breath rate higher more than 30 breath per minute monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause oxygen saturation less than 90% monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause oxygen saturation less than 90% monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause breath rate higher more than 30 breath per minute monitoring for multiparameters monitor of brand phillips;The aplication of insuflation and exsuflation mechanism do not cause oxygen saturation less than 90% monitoring for multiparameters monitor of brand phillips

Secondary

MeasureTime frame
The patients that used cough machine does not have less weaning time, measure in days off mechanical ventilation, compared to patients without cough machine;The patients that used cough machine does not have less lenght of stay, measure in days off mechanical ventilation, compared to patients without cough machine;The patients that used cough machine does not have less aspiration number per day length stay compared to patients without cough machine

Countries

Brazil

Contacts

Public ContactAline Heidemann

Hospital de Clinicas da Unicamp

aline.heidemann@gmail.com+55-019-35217767

Outcome results

None listed

Source: REBEC (via WHO ICTRP)