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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03172169
Other study ID # miRNA and Diaphragm
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 29, 2017
Last updated June 4, 2017
Start date June 15, 2017
Est. completion date December 1, 2017

Study information

Verified date June 2017
Source Southeast University, China
Contact xu xiaoting, master
Phone +86 13645188041
Email xuxiaoting2005@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Through the literature screening of MyomiRX 7, the detection of mechanical ventilation group, difficult withdrawal unit and healthy adult plasma levels of MyomiRX in the evaluation of function and skeletal muscle thickness of the diaphragm, the correlation analysis of 7 kinds of MyomiRX and diaphragmatic dysfunction. The research value of this project is to explore the predictive value of plasma MyomiRX level on diaphragmatic dysfunction in patients with mechanical ventilation, and to lay the foundation for finding the target of VIDD diagnosis and treatment


Description:

1. research content (1) screening MyomiR through literature review (2) selection of mechanical ventilation group, difficult withdrawal units and three healthy adult groups, method for the detection of plasma MyomiRX level and clinical assessment of diaphragmatic function, observation of the relationship between MyomiRX level and diaphragmatic dysfunction, prediction of plasma MyomiRX levels in patients with mechanical ventilation for diaphragmatic dysfunction in value.

2. research objectives Objective to investigate the predictive value of specific minute RNA in plasma muscle tissue on diaphragmatic dysfunction in mechanical ventilation patients Experimental grouping (1) the control group of mechanical ventilation (time of examination, preoperative, admission to ICU and before extubation); (2) difficulty in withdrawal of units (first days, third days and seventh days after the failure of the test time for the first withdrawal); (3) the healthy control group (after the test time was selected)


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 140
Est. completion date December 1, 2017
Est. primary completion date December 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

healthy control group: healthy volunteers mechanical ventilation control group: patients who underwent elective cardiothoracic surgery after scheduled and controlled mechanical ventilation for more than 12h were transferred to ICU (including coronary artery bypass grafting and valve replacement) difficult weaning: difficult to diagnose patients in ICU (weaning time from mechanical ventilation for >48 hours and first SBT failure)

Exclusion Criteria:

1. severe respiratory depression, high paraplegia and neuromuscular lesions;

2. esophageal obstruction, esophageal perforation, severe esophageal varices bleeding, upper gastrointestinal surgery and other reasons can not be placed EAdi catheter;

3. thoracic deformity and diaphragmatic hernia;

4. serious heart, liver, kidney and other organ failure, hemodynamic instability;

5. pregnancy;

6. the end of the tumor or the family member give up the active treatment

Study Design


Related Conditions & MeSH terms

  • Mechanical Ventilation Complication

Intervention

Other:
no Intervention
no Intervention

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Southeast University, China

Outcome

Type Measure Description Time frame Safety issue
Primary Prediction of diaphragmatic dysfunction using RT-PCR microRNA level Prediction of diaphragmatic dysfunction in patients with mechanical ventilation by specific minute RNA of plasma muscle tissue 7 days
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