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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03406676
Other study ID # MZK002
Secondary ID
Status Recruiting
Phase N/A
First received January 4, 2018
Last updated January 22, 2018
Start date August 1, 2017
Est. completion date October 30, 2018

Study information

Verified date January 2018
Source Southwest Hospital, China
Contact Ning Jiaolin, Doctor
Phone 0086-15808014085
Email Njiaolin1976@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To explore the effects of pre-treatment with methylene blue on reduced perioperative vascular resistance in patients with obstructive jaundice.


Description:

Hemodynamic characteristics of patients with obstructive jaundice are high cardiac output, low peripheral vascular resistance. The molecular basis for this feature is the increased production of NO. Methylene blue can increase peripheral resistance, the mechanism is: methylene blue is an oxidoreductase inhibitor, can inhibit the increased production of NO in the vascular endothelium, thereby increasing peripheral vascular resistance.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date October 30, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Aged between 18-60 years;

2. American Society of Anesthesiologists(ASA) grade I~III;

3. TBIL>ULN and TBA>ULN; The patients with obstructive jaundice.

Exclusion Criteria:

1. Organs dysfunction(heart,lungs and etc);

2. Mental disorders;

3. in other clinical trial.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Methylene Blue
2mg / Kg of methylene blue in volume of 50ml is administrated I.V before anesthesia induction.

Locations

Country Name City State
China Southwest Hospital Chongqing Chongqing
China Southwest Hospital Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Southwest Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peripheral vascular resistance the dose of vasoconstrictors used to Maintain Peripheral vascular resistance in the normal range (800 ~ 1200dyns / cm5) through operation completion, an average of 6 hours
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