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OpenTrials
Completed

NCT Number: NCT01147146

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

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

Completed

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Key information

Conditions

Age range

65 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Severance Hospital, Yonsei University College of Medicine

Seoul, South Korea

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

propofol, fentanyl, atracurium

Drug

general anesthesia

Other names: propofol 2mg/kg, fentanyl 50mg, atracurium 0.5mg/kg

Bupivacaine

Drug

spinal anesthesia

Other names: bupivacaine 8-10mg

bupivacaine, Midazolam

Drug

spinal anesthesia & sedation

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

Sponsors and collaborators

Lead sponsor

Yonsei University

Other

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Jun 22, 2010
Registry last updated
May 13, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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