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Completed

NCT Number: NCT01118260

Total Intravenous Anaesthesia (TIVA) Versus Spinal Anaesthesia in Patients Undergoing Transurethral Prostate Resection

Comparison of total intravenous anaesthesia with spinal anaesthesia in patients undergoing transurethral prostate resection

Completed

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Key information

Conditions

Prostate Hyperplasia Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 4

Primary location

Asker & Baerum Hospital

Rud, 1309, Norway

About this study

Comparison of total intravenous anaesthesia with spinal anaesthesia in patients undergoing transurethral prostate resection regarding patient satisfaction and discharge time

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 years and older
  • signed informed consent
  • elective transurethral prostata resection

Exclusion criteria

  • ASA more than 3
  • kidney disease, liver disease
  • intolerance against bupivacaine, fentanyl, propofol og remifentanil
  • chronic pulmonary disease
  • dementia

Treatment and study plan

total intravenous anaesthesia

Procedure

propofol and remifentanil

spinal anaesthesia

Procedure

bupivacaine and fentanyl

Primary outcomes

  1. patient satisfaction

    Time frame: 4 hours

    Patient satisfaction was measured asking the patient about satisfaction with anaesthesia using a 5-point Linkert scale: totally satisfied - satisfied - neither satisfied nor dissatisfied - dissatisfied - totally dissatisfied Time frame: Start anaesthesia to end post anaesthestic care unit

Secondary outcomes

  1. time in PACU

    Time frame: 4 hours

    period in post anaesthetic care unit

Sponsors and collaborators

Lead sponsor

Asker & Baerum Hospital

Other

Registry information

Official study title

TIVA Versus Spinal Anaesthesia in Patients Undergoing Transurethral Prostate Resection

Acronym: TURPS

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
May 6, 2010
Registry last updated
May 6, 2010

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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