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N/A N=46

the Effect of Dopamine on Mechanical Ventilation Induced Lung Injury

Acute Lung Injury

Enrolled (actual)
46
Serious AEs
Results posted
Oct 2018
Primary outcome: Primary: Correlation Coefficient (r) Between Duration of Mechanical Ventilation and DRD1 Expression — -0.555 pearson Correlation Coefficient — p=<0.01

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
mechanical ventilation (Other)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Primary completion
Oct 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Correlation Coefficient (r) Between Duration of Mechanical Ventilation and DRD1 Expression
-0.555 <0.01 sig
SECONDARY
Correlation Coefficient (r) Between Duration of Mechanical Ventilation and DRD2 Expression
0.094 >0.01
SECONDARY
the Expression of TH in Lung Tissues
-0.047 >0.01
SECONDARY
the Expression of DDC in Lung Tissues
-0.012 >0.01
SECONDARY
the Expression of Ac-a-tubulin in Lung Tissues
-0.465 <0.01 sig

Summary

Dopamine(DA) is a common neurotransmitter that has been known to regulate behavior, movement, cardiovascular,endocrine and gastrointestinal functions, but also functions as an important molecule engaging in the immune systems to possess anti-inflammatory effects. However, its role in ventilator-induced lung injury (VILI) is still unclear. Herein, this study aimed to investigate the therapeutic efficacy of dopamine on ventilation-induced lung endothelial barrier dysfunction and explore the possible underlying molecular mechanisms.

Eligibility Criteria

Inclusion Criteria

  • Patients inclusion criteria: undergo elective lobectomy with general anesthesia and mechanical ventilation; classified as physical status I to III according to the American Society of Anesthesiologists Physical Status Classification System; Written informed consent is approved.

Exclusion Criteria

  • Distant metastases: recent anaesthetics or mechanical ventilation treatment;children;women during pregnancy or lactation; being involved in other clinical subjects.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03317431). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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