- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03845556
Clinical Study of Titrating PEEP of Different Methods on Right Heart Function
February 17, 2019 updated by: Chun Pan, Southeast University, China
Clinical Study of Titrating PEEP of Different Methods on Right Heart Function and Pulmonary Artery Pressure in ARDS Patients
To observe the influence of different methods titrating PEEP on right heart function and pulmonary artery pressure in ARDS patients .
Study Overview
Status
Unknown
Conditions
Detailed Description
30 patients who diagnosed as ARDS were included in this study.Then set PEEP with respectively ARDS net 、EIT and Esophageal Pressure in Breathing Machine .
Recorded diameter of right and left ventricular TAM TAPSE pulmonary artery pressure.Objective to evaluate the correlation between the level of PEEP in three methods and the right heart function and pulmonary artery pressure in ARDS patients .
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Jiangsu
-
Nanjing, Jiangsu, China, 210009
- Recruiting
- Zhongda hospital
-
Contact:
- Feng Mei Guo, Dr
- Phone Number: 13813841261
- Email: 13813841261@139.com
-
Principal Investigator:
- FengMei Guo, Dr
-
-
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
18 years to 80 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Population admitted to ICU of Zhongda hospital,diagnosed of medium or serious ARDS。
Description
Inclusion Criteria:
- Patients admitted to ICU diagnosed of modecate to severe ARDS (Berlin criteria)
- Patients age between 18 years old and 80 years
Exclusion Criteria:
- Patients with chronic respiratory diseases such as COPD.
- Ventilated because of oesophageal surgery in the previous 12months.
- Patients who cannot obtain clear ultrasound images due to thoracic surgery ,massive pleural effusion.
- Oesophageal bleeding in previous 30 days history of oesophageal varices.
- Facial trauma and surgery.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the function of right heart and pulmonary artery pressure
Time Frame: 2018.4-2019.3
|
Systolic Pulmonary Artery Pressure TAPSE or Tricuspid Annular Motion orTricuspid annular plane systolic excursion or right ventricular diameter or right left ventricular diameter ratio in diffrient PEEP
|
2018.4-2019.3
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Chun Pan, 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 (ACTUAL)
August 4, 2018
Primary Completion (ANTICIPATED)
March 30, 2019
Study Completion (ANTICIPATED)
March 30, 2019
Study Registration Dates
First Submitted
October 11, 2018
First Submitted That Met QC Criteria
February 17, 2019
First Posted (ACTUAL)
February 19, 2019
Study Record Updates
Last Update Posted (ACTUAL)
February 19, 2019
Last Update Submitted That Met QC Criteria
February 17, 2019
Last Verified
February 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ARDS
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.