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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03762538
Other study ID # EAGLES
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 1, 2019
Est. completion date December 31, 2019

Study information

Verified date January 2018
Source Shanghai Zhongshan Hospital
Contact Kefang Guo, MD
Phone +86-13817706936
Email drguokefang@foxmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to determine whether ALDH2 gene polymorphisms (G/G, G/A A/A) have effect on the potency of propofol.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 31, 2019
Est. primary completion date June 30, 2019
Accepts healthy volunteers No
Gender Male
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- ASA II

Exclusion Criteria:

- ASA III-IV

- OSAS

- hepatic and renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Propofol
Patients will be induced to unconsciousness using propofol intravenously.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Effect-site concentration patient's effect-site concentration when he/she loss consciousness immediately after patient lose his/her consciousness
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