ClinicalTrials.Veeva

Menu

Performance of Novel Bed Side Scores as Predictors of Hospital Outcome in Acute Exacerbation of Chronic Obstructive Pulmonary Disease Among Women; Cohort Study

A

Assiut University

Status

Not yet enrolling

Conditions

COPD Exacerbation

Study type

Observational

Funder types

Other

Identifiers

NCT05370664
Mortality outcome in COPD

Details and patient eligibility

About

  • Assess predictors of mortality in COPD exacerbation between men and women.
  • Evaluate the clinical outcomes in acute exacerbation of COPD in women.
  • Evaluate the validity of new scoring systems ( NIVO, DECAF, HACOR ) as a predictor for hospital outcome in acute exacerbation of COPD.
  • Compare these new scoring system with the most widely used APACHE IV.
  • Assessment of serum level of granulocyte colony stimulating factor ( GM-CSF) in detecting the severity of COPD exacerbation.

Enrollment

203 estimated patients

Sex

All

Ages

35+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with AECOPD leading to hypoxemia, hypercapnia and respiratory acidosis with pH < 7.35 and PaCO2 > 45 mm of Hg will be admitted to the respiratory intensive care unit (ICU) for NIV or the ward will be eligible for inclusion and not in need for mechanical ventilation

Exclusion criteria

  • Requirement for emergency intubation.
  • Other contraindications to NIPPV including cardiac or respiratory arrest; nonrespiratory organ failure (eg, severe encephalopathy, severe gastrointestinal bleeding, hemodynamic instability with or without unstable cardiac angina); facial surgery or trauma; upper-airway obstruction; inability to protect the airway and/or high risk of aspiration; and inability to clear secretions.(6)
  • Age < 35 years.

Trial design

203 participants in 2 patient groups

Female COPD
Male COPD

Trial contacts and locations

0

Loading...

Central trial contact

Khaled Essmat Hussien, MSSH; Sahar Refaat Mahmoud, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems