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Sponsored by: |
University of Schleswig-Holstein |
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Information provided by: | University of Schleswig-Holstein |
ClinicalTrials.gov Identifier: | NCT00591435 |
Anaesthesia and surgery related time intervals of three standard operations are compared depending on whether residents or consultants are performing anaesthesia and surgery. Hypothesis: Perioperative workflow is influenced by state of education, time intervals reflecting anaesthesia as well as surgical performance increase due to resident training. Therefore, costs of perioperative care increase as well.
Condition | Intervention |
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Intraoperative Workflow Anesthesia and Procedure Related Time Intervals |
Other: Comparison of performance of consultants versus residents |
Study Type: | Observational |
Study Design: | Cohort, Retrospective |
Official Title: | Resident Training Affects Intra-Operative Workflow and Costs |
Enrollment: | 600 |
Study Start Date: | January 2007 |
Study Completion Date: | December 2007 |
Primary Completion Date: | December 2007 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
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1
200 laparoscopic cholecystectomies will be included, consultant cases will be compared to resident cases
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Other: Comparison of performance of consultants versus residents
Anesthesia as well as surgical workflow will be analysed. Performance of consultants will be compared to residents
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2
200 laparoscopic pelviscopies will be included, consultant cases will be compared to resident cases
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Other: Comparison of performance of consultants versus residents
Anesthesia as well as surgical workflow will be analysed. Performance of consultants will be compared to residents
|
3
200 transurethral resection of urinary bladder or prostate gland will be included, consultant cases will be compared to resident cases
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Other: Comparison of performance of consultants versus residents
Anesthesia as well as surgical workflow will be analysed. Performance of consultants will be compared to residents
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Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Healthy subjects scheduled for one of the three defined procedures (defined by German Diagnose Related Groups ID) under general or regional anesthesia
Inclusion Criteria:
Exclusion Criteria:
Germany, Schleswig-Holstein | |
University Hospital Schleswig-Holstein, Campus Kiel | |
Kiel, Schleswig-Holstein, Germany, 24105 |
Principal Investigator: | Jens Scholz, MD, Professor | Department of Anaesthesiology and Intenisve Care Medicine, University Hospital Schleswig-Holstein, Campus Kiel |
Responsible Party: | ( Jens Scholz, Professor of Anaesthesiology, Chair of the Department of Anaesthesiology and Intensive Care Medicine ) |
Study ID Numbers: | UKSH_Hanss, IRB: A138/07 |
Study First Received: | December 28, 2007 |
Last Updated: | December 28, 2007 |
ClinicalTrials.gov Identifier: | NCT00591435 History of Changes |
Health Authority: | Germany: Ethics Commission |
Anesthesia Surgery Education Economics |
Anesthetics |