ClinicalTrials.Veeva

Menu

ROX Index Versus MROX Index to Predict Treatment Outcome for High Flow Nasal Cannula And/or Noninvasive Ventilation in Patients with Respiratory Failure

A

Assiut University

Status

Not yet enrolling

Conditions

Respiratory Failure

Study type

Observational

Funder types

Other

Identifiers

NCT06715644
ROX mROX HFNC RF

Details and patient eligibility

About

One of managing steps in respiratory failure is high flow nasal cannula (HFNC), but the exact time to turn to invasive machine ventilation (IMV) is necessarily being determined. Respiratory rate and oxygenation (ROX) index, defined as the ratio of oxygen saturation as measured by pulse oximetry (SO2)/ FiO2 to respiratory rate (RR), is used to determine when to intubate the patients who are on HFNC and prevent the delayed intubation. Modified Respiratory rate and oxygenation (mROX), defined as (PaO2/ FiO2) / respiratory rate, is also used to point the time of intubation in case HFNC of patients with respiratory failure . The diagnostic and prognostic accuracy of both parameters are reported in previous papers, but the preference of them is under research. In this study, we aim to observe and compare the diagnostic accuracy between ROX and mROX in determine the time of invasive mechanical ventilation.

Full description

Respiratory Failure (RF) is a condition where there's insufficient oxygenation in the body tissue, whether acute, chronic or acute on chronic; occurring due to decreased oxygen or excessive carbon-dioxide in the blood . There are four types of respiratory failure; Hypoxemic respiratory failure (Type1), hypercapnic respiratory failure (Type2), ) . Causes of RF are varied and accounted for any abnormality related upper respiratory tract, lower respiratory tract, central and peripheral nervous system or muscles of respiration . However, in the last three decades, the most common causes of RF is acute myocardial infarction (AMI), acute respiratory distress syndrome (ARDS), RF related to corona virus (Covid-19) and acute exacerbation of chronic obstructive lung disease (COPD).

Enrollment

120 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients of both sex aged between 18 to 80 years
  • Patient diagnosed with acute type 1or 2 or chronic type 1or 2 respiratory failure.
  • Patient for chest ICU admission
  • Patient for HFNC and/ or Noninvasive mechanical ventilation.

Exclusion criteria

  • Pediatric patients
  • Pregnant females
  • Patients who are for intubation on ICU admissionc.

Trial design

120 participants in 2 patient groups

group 1
Description:
patients with respiratory failure treated with high flow nasal cannula
group 2
Description:
patients with respiratory failure treated with noninvasive ventilation in

Trial contacts and locations

0

Loading...

Central trial contact

Esraa Ramadan Abd el rahman Ibraheim, resident doctor

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems