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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03213743
Other study ID # 1stKunmingMCQJQ
Secondary ID
Status Completed
Phase N/A
First received July 7, 2017
Last updated July 10, 2017
Start date June 19, 2017
Est. completion date June 21, 2017

Study information

Verified date July 2017
Source The First Affiliated Hospital of Kunming Medical College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to find out the differential expression profiling of microRNA before and after adiministration of dexmedetomidine in patients undergoing procedures, and then investigators will do some in vitro studies to validate the functions of the microRNA.


Description:

Background and objective: The use of dexmedetomidine may have benefits on the clinical outcomes of cardiac surgery. MicroRNAs are non-coding RNA sequences that act as regulators of gene expression. Investigators conduct a study to determine the role of microRNAs in cardioprotection mediated by dexmedetomidine.

Methods: In this study 3 patients were selected. The blood sample were taken before administration of dexmedetomidine.Investigators infused loading dose of dexmedetomidine for 10 minutes and maintaining dese of dexmedetomidine for 20 minutes.Thirty minutes after the administration, another blood samples were taken and stored in the liquid nitrogen and both the samples were marked. Those sample were analyzed for differentially expressed microRNA with Exiqon miRNA Array.


Recruitment information / eligibility

Status Completed
Enrollment 3
Est. completion date June 21, 2017
Est. primary completion date June 21, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

- The patients without arrithmia will undergo procedure.

Exclusion Criteria:

- The patients have bradycardia (hear rate is less than 60 beats per minute) or conduction block.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexmedetomidine Injection
Investigators gave the patients loading dose of dexmedetomidine for 10 minutes and maintaining dose of dexmedetomidine for 20 minutes. Investigators took blood samples before and after the administration of dexmedetomidine.

Locations

Country Name City State
China Jinqiao Qian Kunming Yunnan

Sponsors (1)

Lead Sponsor Collaborator
The First Affiliated Hospital of Kunming Medical College

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary microRNA differential expression microRNA differential expression exerts cardioprotection effect on patients undergoing procedures. 30 minutes
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