- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02487927
The Classification of Difficult Weaning and the Predictive Value of Relative Factors for Difficult Weaning
June 29, 2015 updated by: Jianfeng Xie
To evaluate the distribution of different types of difficult weaning and the predictive value of weaning relative factors.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
108 patients who passed the spontaneous breathing test (SBT) were included in this study,every patient were performed 30-60 minutes SBT after enrollment.Patients were divided into succeed weaning and difficult weaning group according the results of SBT, the difficult weaning group were futher divided into A(Airway and Lung dysfunction),B(Brain dysfunction),C(Cardic dysfunction),D(Diaphragm dysfunction),E(Endocrine and metabolic dysfunction)five different groups according to the causes of difficult weaning.
The respiratory mechanical parameters,the diameter of inferior vena cava and the diaphgram excursion were recorded before SBT and 30 minutes after SBT.
Study Type
Observational
Enrollment (Anticipated)
110
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jianfeng Xie, Dr
- Phone Number: +862583262550
- Email: panchun1982@gmail.com
Study Locations
-
-
Jiangsu
-
Nanjing, Jiangsu, China, 210009
- Recruiting
- Zhongda Hospital
-
Contact:
- Haibo Qiu, Prof
- Phone Number: +862583262550
- Email: haiboq2000@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 80 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
mechanical vetilation patients in ICU, and the patients are weaninng candidates
Description
Inclusion Criteria:
- mechanical ventilation patients
- prepared to weaning
- sign on the acknowledged
Exclusion Criteria:
- endotracheotomy
- single lung
- pregnant
- heart,liver,renal failure
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Weaning success
patients pass SBT and weaning without any ventilation in 48 hours
|
T piece
|
weaning failure
patients do not pass SBT or ventilation with any ventilation in 48 hours
|
T piece
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the reasons of difficult weaning
Time Frame: 30 mins
|
30 mins
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The predictive value of diaphragm associated values in weaning
Time Frame: 30mins
|
30mins
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Haibo QIU, Dr, Southeast university
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2012
Primary Completion (Anticipated)
July 1, 2015
Study Completion (Anticipated)
July 1, 2015
Study Registration Dates
First Submitted
June 23, 2015
First Submitted That Met QC Criteria
June 29, 2015
First Posted (Estimate)
July 2, 2015
Study Record Updates
Last Update Posted (Estimate)
July 2, 2015
Last Update Submitted That Met QC Criteria
June 29, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- Weaning Study
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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