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Preoperative Noninvasive Hemoglobin Monitoring in Pediatric Patients

The Accuracy of the Noninvasive Hemoglobin Monitoring for Preoperative Evaluation for Pediatric Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02484365
Enrollment
177
Registered
2015-06-29
Start date
2014-12-31
Completion date
2019-03-31
Last updated
2018-07-18

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

Conditions

Surgery

Keywords

Hemoglobins, Monitoring, Outpatient, Preoperative Period, Pediatrics

Brief summary

The preoperative evaluation including sampling blood in pediatric patients is hard to perform. However, the knowledge of the baseline cell blood count is important to prepare unexpected surgical bleeding etc.. The invasive procedure for blood sampling in small children is often failed and sometimes induces iatrogenic blood loss and parent's complaints. The Pulse Co-oximetry (Masimo) is recently developed device which can provide noninvasive hemoglobin value. However, the accuracy is controversial. There are studies in pediatric patients during surgery and in ICU. However, the comparison for preoperative evaluation is not analysed. Therefore, the investigators want to evaluate the accuracy for preoperative preparation in pediatric patients.

Detailed description

There are not enough data comparing the noninvasive hemoglobin and venous hemoglobin in pediatric patients during preoperative period. The investigators will collect the venous sample and the noninvasive hemoglobin data from masimo within 1 hour. Without any additional medication, the patients will visit preanesthetic room and attach the probe of masimo on index finger. The R 20L or R25L will be used based on their weight. The parameter will be stabilized within 2 minutes and the SpHb and perfusion index will be recorded.

Interventions

OTHERNo treatment

Attach adhesive probe on thumb or index finger

Sponsors

Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* ASA class 1,2

Exclusion criteria

* Poor peripheral circulation * Infection or trauma on the sensor contact region

Design outcomes

Primary

MeasureTime frameDescription
hemoglobinonce, preoperative visit anesthetic officeno F/U is needed

Countries

South Korea

Contacts

Primary ContactYong-Hee Park
dada822@naver.com82

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026