NCT05738928

Brief Summary

Identification of the microbial profile of Ventilator associated pneumonia causing microorganisms among Respiratory ICU patients .

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
86

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2023

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2023

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

February 13, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 22, 2023

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2023

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2024

Completed
Last Updated

February 22, 2023

Status Verified

February 1, 2023

Enrollment Period

10 months

First QC Date

February 13, 2023

Last Update Submit

February 13, 2023

Conditions

VAP - Ventilator Associated Pneumonia

Outcome Measures

Primary Outcomes (1)

  • Microbiological profile of ventilator associated pneumonia in Respiratory ICU in Assiut University Hospital.

    Identify the microbial profile of VAP causing microorganisms among ICU patients, antimicrobial susceptibility patterns among the frequently isolated organisms and resistant strains.

    1 year

Interventions

blood and sputum cultureDIAGNOSTIC_TEST

Noninvasive sampling ( Endo Tracheal Aspiration) for staining and culture. Blood culture .

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Age more than 18 years. Mechanically ventilated patient who developed pneumonia after48 hours after endotracheal intubation.

You may qualify if:

  • Mechanically ventilated patient who developed pneumonia after48 hours after endotracheal intubation.
  • Age \> 18 years.

You may not qualify if:

  • Patients with clinical and radiological signs suggestive of pneumonia before intubation (community acquired pneumonia or hospital acquired pneumonia)
  • Patients age ≤18 years old

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pneumonia, Ventilator-Associated

Interventions

Blood Specimen Collection

Condition Hierarchy (Ancestors)

Healthcare-Associated PneumoniaCross InfectionInfectionsPneumoniaRespiratory Tract InfectionsLung DiseasesRespiratory Tract DiseasesIatrogenic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Specimen HandlingClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisPuncturesSurgical Procedures, OperativeInvestigative Techniques

Study Officials

  • mohammed M Abdelhadi, PhD

    Assiut University

    STUDY DIRECTOR

Central Study Contacts

Manar A Hassan, bacheoler

CONTACT

+201152808012manarabdelhameed89@yahoo.com

Manar A hassan, diploma

CONTACT

*201007090074manarabdelhameed89@gmail.com

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor

Study Record Dates

First Submitted

February 13, 2023

First Posted

February 22, 2023

Study Start

February 1, 2023

Primary Completion

December 1, 2023

Study Completion

February 1, 2024

Last Updated

February 22, 2023

Record last verified: 2023-02