Suspended

IAP_SBTMeasuring the Change of Intra-abdominal Pressures of the Intensive Care Unit Patients During the Spontaneous Breathing Trial

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Respiration Disorders

+ Respiratory Tract Diseases

+ Respiratory Insufficiency

From 18 to 90 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: January 2012
See protocol details

Summary

Principal SponsorNational Taiwan University Hospital
Study ContactNin-Chieh Hsu, MDMore contacts
Last updated: February 22, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2012

Actual date on which the first participant was enrolled.

During the weaning process, we tapered down the respiratory support from mechanical ventilation and recruited respiratory muscles to work. Previous study showed that transdiaphragmatic pressure was increasing while pressure support was reducing. However, the transdiaphragmatic pressure required invasive procedure to measure and not used frequently in weaning. IAP reflects the pleural pressure. If the PEEP is not changed, change of IAP is largely due to change of transpulmonary pressure. Study Aim: To evaluate the patterns of change of IAP during SBT To predict success of SBT by the change of IAP To predict weaning outcome by the change of IAP

NCT01797614
Principal SponsorNational Taiwan University Hospital
Study ContactNin-Chieh Hsu, MDMore contacts
Last updated: February 22, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

100 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 90 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Respiration DisordersRespiratory Tract DiseasesRespiratory Insufficiency

Criteria

2 inclusion criteria required to participate
Adult patients with endotracheal intubation in the intensive care unit
The clinical condition is considered to prepare for weaning assessment
6 exclusion criteria prevent from participating
baseline IAP above 20 mmHg
no foley catheter in place or had been removed
poor cooperation due to agitation
severe heart failure, heart disease or arrhythmia
Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Recruiting

National Taiwan University Hospital

Taipei, TaiwanOpen National Taiwan University Hospital in Google Maps
Recruiting soon

Nin-Chieh Hsu

Taipei, Taiwan
Suspended2 Study Centers