The Effects of Anesthetic Method on Cerebral Oxygen Saturation in Geriatric Patients Undergoing Transurethral Surgery

This study has been completed.

Sponsor:

Information provided by:

Yonsei University

ClinicalTrials.gov Identifier:

NCT01147146

First received: June 17, 2010

Last updated: May 12, 2011

Last verified: May 2011

History of Changes

Tracking Information

First Received Date ^ICMJE

June 17, 2010

Last Updated Date

May 12, 2011

Start Date ^ICMJE

June 2010

Primary Completion Date

December 2010 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

Not Provided

Original Primary Outcome Measures ^ICMJE

Not Provided

Change History

Complete list of historical versions of study NCT01147146 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Not Provided

Original Secondary Outcome Measures ^ICMJE

Not Provided

Current Other Outcome Measures ^ICMJE

Not Provided

Original Other Outcome Measures ^ICMJE

Not Provided

Descriptive Information

Brief Title ^ICMJE

The Effects of Anesthetic Method on Cerebral Oxygen Saturation in Geriatric Patients Undergoing Transurethral Surgery

Official Title ^ICMJE

The Effects of Anesthetic Method on Cerebral Oxygen Saturation in Geriatric Patients Undergoing Transurethral Surgery

Brief Summary

The effects of anesthetic method on cerebral oxygen saturation in geriatric patients undergoing transurethral surgery.

Detailed Description

Not Provided

Study Type ^ICMJE

Interventional

Study Phase

Not Provided

Study Design ^ICMJE

Allocation: Randomized
Primary Purpose: Prevention

Condition ^ICMJE

Surgery

Intervention ^ICMJE

Drug: propofol, fentanyl, atracurium
general anesthesia

Other Name: propofol 2mg/kg, fentanyl 50mg, atracurium 0.5mg/kg
Drug: bupivacaine
spinal anesthesia

Other Name: bupivacaine 8-10mg
Drug: bupivacaine, Midazolam
spinal anesthesia & sedation

Other Name: Bupivacine 8-10mg, Midazolam 0.5mg/kg

Study Arm (s)

Not Provided

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Enrollment ^ICMJE

Completion Date

December 2010

Primary Completion Date

December 2010 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

male patients (ASA physical status I and II) aged over 65 yrs and scheduled elective transurethral surgery

Exclusion Criteria:

cardiovascular, renal, liver disease, or cerebrovascular disorder

Gender

Male

Ages

65 Years and older

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

Korea, Republic of

Administrative Information

NCT Number ^ICMJE

NCT01147146

Other Study ID Numbers ^ICMJE

4-2010-0133

Has Data Monitoring Committee

Yes

Responsible Party

Jeong-Yeon Hong / Associate Clinical Professor, Yonsei University, College of Medicine

Study Sponsor ^ICMJE

Yonsei University

Collaborators ^ICMJE

Not Provided

Investigators ^ICMJE

Principal Investigator:

Jeong-Yeon Hong, MD

Anesthesiology & Pain Medicine, Severance Hospital

Information Provided By

Yonsei University

Verification Date

May 2011

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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