Can the Usage of Regional Block Room Save the Time of Anesthesia Team
1 other identifier
observational
800
1 country
1
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?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2011
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2011
CompletedFirst Submitted
Initial submission to the registry
December 7, 2011
CompletedFirst Posted
Study publicly available on registry
December 26, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2012
CompletedDecember 26, 2011
December 1, 2011
7 months
December 7, 2011
December 22, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
anesthesia-controlled time
anesthesia-controlled time = anesthesia pre-procedure time + anesthesia post-procedure time
3 months
Secondary Outcomes (2)
turnover time
3 months
number of elective cases after 4PM
3 months
Study Arms (2)
RA in block room
Performing regional anesthesia in the block room
RA inside OR
Performing regional anesthesia inside the main orthopedic operating room
Interventions
regional anesthesia procedure
Eligibility Criteria
elective orthopedic surgical patients that require for anesthesia
You may qualify if:
- elective orthopedic surgical patients that require for anesthesia ( start 9AM-4PM)
You may not qualify if:
- surgery under local infiltration
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Medicine Siriraj Hospital, Mahidol University
Bangkok, Bangkok, 10700, Thailand
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Suwimon Tangwiwat, M.D
Mahidol University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 7, 2011
First Posted
December 26, 2011
Study Start
October 1, 2011
Primary Completion
May 1, 2012
Study Completion
July 1, 2012
Last Updated
December 26, 2011
Record last verified: 2011-12