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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02516943
Other study ID # Si 723/2557(EC4)
Secondary ID
Status Completed
Phase Phase 4
First received August 4, 2015
Last updated December 10, 2015
Start date November 2014
Est. completion date May 2015

Study information

Verified date December 2015
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

Blood gas analysis were routinely monitor every 4 hours in our surgical cardiac intensive care unit (SICU). These luxury investigations waste the resources. Therefore we develop a pathological- based guideline for arterial blood gas analysis in patients after cardiac surgery. We test the guideline for its safety and efficacy.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient undergone elective cardiac surgery with cardiopulmonary bypass

Exclusion Criteria:

- Emergency surgery

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
Control
The patient's ABGs were test according to a 4 - hour routine
Guideline
The patient's ABGs were test according to the guideline for requests Arterial Blood Gas status post cardiac surgery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Outcome

Type Measure Description Time frame Safety issue
Primary Number of ABG test during intensive care stay 14 days Yes
Secondary Influence of ABG testing on patients' outcome. during intensive care stay 14 days Yes
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