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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05171296
Other study ID # FMASU R 177 / 2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 22, 2021
Est. completion date August 22, 2022

Study information

Verified date July 2022
Source Ain Shams University
Contact Amr hafez, M.D
Phone 01225674370
Email amr_foud@med.asu.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We aimed to study the efficacy of Noninvasive Hemoglobin Monitoring by Spectrophotometry in monitoring hemoglobin level in trauma patients for conservative management.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date August 22, 2022
Est. primary completion date August 22, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - American Society of Anesthesiologists (ASA) physical status I to III, of either sex, 18 -80 years of age, non-sedated non-intubated patients who will be admitted to Ain Shams university hospital - surgical intensive care unit, after blunt abdominal trauma planned for conservation. Exclusion Criteria: - Patients with fever, hypothermia, history of a neurological, psychiatric, dementia or, who are taking psychotropic drugs Patients with unstable hemodynamic status, and unconscious patients.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Ain Shams University hospitals Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary accuracy of hemoglobin measured by the noninvasive device. accuracy of hemoglobin measured by the noninvasive hemoglobin test device (Radical-7®; Masimo Corp., Irvine, CA) in comparison with standard CBC that is assayed on Coulter LH 750 Cell Counter (Beckman Coulter Corporation, Florida, USA), using reagents supplied by the company in patients suffering frm blunt abdominal trauma aditted to ICU for observation. 3 months
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