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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03271502
Other study ID # 2017-1011
Secondary ID
Status Completed
Phase N/A
First received August 31, 2017
Last updated October 25, 2017
Start date September 4, 2017
Est. completion date October 1, 2017

Study information

Verified date October 2017
Source Asan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study was to evaluate the difference between the optic nerve sheath diameter measured during total intravenous anesthesia and the optic nerve sheath diameter measured during inhalation anesthesia in patients undergoing robot-assisted laparoscopic prostatectomy.


Description:

The purpose of this study was to evaluate the difference between the optic nerve sheath diameter measured during total intravenous anesthesia with propofol and remifentanil and the optic nerve sheath diameter measured during inhalation anesthesia with sevoflurane and remifentanil in patients undergoing robot-assisted laparoscopic prostatectomy.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date October 1, 2017
Est. primary completion date September 26, 2017
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 79 Years
Eligibility Inclusion Criteria:

Patients who have undergone a robot-assisted laparoscopic prostatectomy with a prostate cancer and who are 20 years of age or older and under 80 years of age and who agree to participate in this study.

Exclusion Criteria:

Patients with a history of cerebral hemorrhage or cerebral infarction, Patients < 20 years of age, Patients = 80 years of age, Patients with unexpected hemodynamic instability during surgery, Failure to measure optic nerve sheath diameter.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Total intravenous anesthesia
Total intravenous anesthesia with propofol and remifentanil
Inhalation anesthesia
Inhalation anesthesia with sevoflurane and remifentanil

Locations

Country Name City State
Korea, Republic of Asan Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Asan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in optic nerve sheath diameter Difference between the optic nerve sheath diameter measured during total intravenous anesthesia and the optic nerve sheath diameter measured during inhalation anesthesia 60 minutes after pneumoperitoneum and steep Trendelenburg position
Secondary Difference in optic nerve sheath diameter Difference between the optic nerve sheath diameter measured during total intravenous anesthesia and the optic nerve sheath diameter measured during inhalation anesthesia 30 minutes after pneumoperitoneum and steep Trendelenburg position
Secondary Difference in optic nerve sheath diameter Difference between the optic nerve sheath diameter measured during total intravenous anesthesia and the optic nerve sheath diameter measured during inhalation anesthesia 5 minutes after pneumoperitoneum and steep Trendelenburg position
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