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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02575443
Other study ID # ADMS NMD depth
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2015
Est. completion date September 2017

Study information

Verified date October 2018
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluated whether the depth of neuromuscular block may affect the unicon value of anesthetic depth monitoring system (ADMS).


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Gall bladder disease

- American Society of Anesthesiologist physical status 1 or 2

Exclusion Criteria:

- Pregnancy

- Body mass index < 16

- Body mass index >30

- Neuromuscular disease

- Previous intraabdominal surgery

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Rocuronium (MB group)
Count of train-of-four: 1-2 Titration of rocuronium dose
Rocuronium (DB group)
Post-tetanic count: 1-2 Titration of rocuronium dose

Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam Gyeonggi

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total infused dose of propofol At 1 min after the anesthesia is finished
Secondary Electromyographic index presented on the anesthetic depth monitoring system Through study completion, an average of 2 hours
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