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Clinical Trials/NCT01499589
NCT01499589UnknownNot Applicable

Can the Usage of Regional Block Room Save the Time of Anesthesia Team in the Main Orthopedic Operating Room?

Mahidol University1 site in 1 country800 target enrollmentStarted: October 2011Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
800
Locations
1
Primary Endpoint
anesthesia-controlled time
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Study of time usage of anesthesia team inside the main operating room compares between 2 groups of

  • Performing regional anesthesia inside the operating room
  • Performing regional anesthesia in the block room

Study purpose: How much will the investigators save time in the main operating room if we perform the regional anesthesia in the block room?

Detailed Description

Anesthesia-controlled time means anesthesia pre-procedure time plus anesthesia post-procedure time.

We also compares the anesthesia-controlled time in 3 groups of

  • general anesthesia
  • regional anesthesia
  • general anesthesia combined with regional anesthesia

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
1 Month to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •elective orthopedic surgical patients that require for anesthesia ( start 9AM-4PM)

Exclusion Criteria

  • •surgery under local infiltration

Outcomes

Primary Outcomes

anesthesia-controlled time

Time Frame: 3 months

anesthesia-controlled time = anesthesia pre-procedure time + anesthesia post-procedure time

Secondary Outcomes

  • turnover time(3 months)
  • number of elective cases after 4PM(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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