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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03561831
Other study ID # KUH1160108
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 5, 2018
Est. completion date May 29, 2019

Study information

Verified date October 2021
Source Konkuk University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigate the change in endoplasmic reticulum stress after cancer surgery according to different anaesthetics including propofol and sevoflurane.


Description:

We hypothesize propofol and sevoflurane based anesthesia would show different pattern of endoplasmic reticulum stress after cancer surgery in patients with cancer


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date May 29, 2019
Est. primary completion date May 29, 2019
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria: - patients with cancer Exclusion Criteria: - age under 19 years old - allergy history to propofol or sevoflurane - history of previous cancer

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Propofol
propofol based anesthesia
Sevoflurane
sevoflurane based anesthesia

Locations

Country Name City State
Korea, Republic of Konkuk University Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Konkuk University Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in endoplasmic reticulum stress Change in endoplasmic reticulum stress baseline, postoperative 1 hours and 24 hours
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