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Role of i-STAT system in reducing time to treatment-decision making in urgency patients

Role of i-STAT system in reducing time to treatment-decision making in urgency patients: a randomized trial and cost effectiveness analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170324005
Enrollment
Unknown
Registered
2017-03-24
Start date
2017-04-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Time to decision making Emergency department length of stay Cost effectiveness

Interventions

Nursing staffs who have received training on how to operate the i&#45
STAT system before beginning the study will draw same amount of blood volume as to that of the central laboratory test group for patients in the i&#45
STAT testing group. The providers will insert 2 or 3 drops of blood into the CHEM 8+ cartridge (including sodium&#44
potassium&#44
chloride&#44
ionized calcium&#44
total CO2&#44
glucose&#44
blood urea nitrogen (BUN) and creatinine). The cartridge will be inserted into the handheld device and the results will be viewed from the device in a time period of 2 minutes and printed with the por
STAT will be attached to OPD card and scanned into Si&#45
IT system. The nursing staff will report the results to the same physician as soon as possible. In case&#44
the ordered blood testing requires certain blood profiles which are not included in CHEM 8+&#44
the remaining blood sample will be delivered to the central laboratory. When both results are reported&#44
the nursing staff will notify the same physicians as soon as possible.,For the patients in the Central laboratory testing group&#44
the nurses will draw blood as per the usual requisites. When the results have been reported by the laboratory&#44
the nurses will notify the physician on duty.
STAT testing,Central laboratory testing

Sponsors

Human Research Protection Program of Faculty of Medicine, Siriraj Hospital
Lead Sponsor
Transmedic Thailand Co. ltd. 888/70 7th Floor&#44
Collaborator
Mahatun Plaza Building
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Age>/= 18 years - Patients who are classified as urgent patients with Siriraj Adult Triage System (level 3 and 4) - Patients who are clinically required to have chemistry laboratory tests (at least electrolyte: Sodium Potassium Chloride Bicarbonate)

Exclusion criteria

Exclusion criteria: - Pregnancy (considered as vulnerable population) - Trauma (patients would be receiving medical services from the Trauma Center, not Urgency Room) - Bedridden patients (these patients would be requiring prolonged hospital stay)

Design outcomes

Primary

MeasureTime frame
Time to Treatment Decision Making and ED-LOS time 3 months Mann-Whitney-Wilcoxon test. Other categorical variables will be compared with chi-square tests.

Secondary

MeasureTime frame
Cost effectiveness and Provider and Patient satisfaction form 3 months Incremental cost effectiveness ratio, Provider and Patient satisfaction form

Countries

Thailand

Contacts

Public ContactWansiri Chaisirin

Department of Emergency Medicine, Siriraj Hospital

talk2yam@hotmail.com0815617822

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026