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NCT01499589 Clinical Trial

Can the Usage of Regional Block Room Save the Time of Anesthesia Team

Anesthesia Clinical Trial

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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01499589
Other study ID # Si562/2011
Secondary ID
Status Recruiting
Phase N/A
First received December 7, 2011
Last updated December 22, 2011
Start date October 2011
Est. completion date July 2012

Study information
Verified date December 2011
Source Mahidol University
Contact Suwimon Tangwiwat, M.D
Phone (66)81-645-6167
Email stangwiwat@yahoo.com
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Observational

Clinical Trial 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?

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

Recruitment information / eligibility
Status Recruiting
Enrollment 800
Est. completion date July 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group 1 Month and older
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

- surgery under local infiltration

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• regional anesthesia
regional anesthesia procedure

Locations
Country Name City State
Thailand Faculty of Medicine Siriraj Hospital, Mahidol University Bangkok

Sponsors (1)
Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary anesthesia-controlled time anesthesia-controlled time = anesthesia pre-procedure time + anesthesia post-procedure time 3 months No
Secondary turnover time turnover time = time new patient-in minus previous patient-out 3 months No
Secondary number of elective cases after 4PM number of the elective cases that will be running after 4 PM 3 months No
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