Nosocomial Bacterial and Fungal Chest Infections in Cirrhotic Patients
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| ClinicalTrials.gov Identifier: NCT03413293 |
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Recruitment Status : Unknown
Verified February 2018 by NZBakhiet, Assiut University.
Recruitment status was: Not yet recruiting
First Posted : January 29, 2018
Last Update Posted : May 18, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Nosocomial Infection | Diagnostic Test: Diagnosis of bacterial infections |
Aim of the work
- To estimate the frequency and risk factors of nosocomial chest infections in cirrhotic patients .
- To determine the causative pathogens of nosocomial chest infections in patients with cirrhosis including fungal infections in order to establish our local empirical antimicrobial protocol.
- To define the impact of nosocomial chest infections on survival of our patients.
- To develop an effective and continuous surveillance program and infection control measures to reduce the burden of these infections as well as morbidity , mortality , hospital stay ,hospital cost and to achieve quality of care .
- To motivate pharmaceutical companies to create a new umbrella coverage of antimicrobials through the ongoing knowledge of the changes in microbial resistance pattern inside hospitals
| Study Type : | Observational |
| Estimated Enrollment : | 20 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Prospective |
| Official Title: | Nosocomial Bacterial and Fungal Chest Infections in Cirrhotic Patients |
| Estimated Study Start Date : | June 2018 |
| Estimated Primary Completion Date : | May 2019 |
| Estimated Study Completion Date : | August 2019 |
| Group/Cohort | Intervention/treatment |
|---|---|
| Nosocomial infected cirrhotic patients |
Diagnostic Test: Diagnosis of bacterial infections
Cultures |
- Frequency of nosocomial infection in patients with liver cirrhosis [ Time Frame: baseline ]nosocomial infection is one of predictors of bad outcome in liver cirrhosis
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- All cirrhotic patients , decompensated , child pug score B or C ,may have Hepatocellular carcinoma , other comorbidities may present as (Diabetius mellitus , Hypertension , Heart disease and renal impairment ) , both sex and with clinical suspicion of chest infections acquired after 48 hours of admission
Exclusion Criteria:
- Patients have any chronic chest disease
- Patients have severe immunosuppression (neutropenia after chemotherapy or hematopoietic transplant, drug-induced immunosuppression in solid-organ transplant or cytotoxic therapy, and HIV-related disorders.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03413293
| Contact: Nariman zaghluol bakhiet, postgraduate | 01005546130 | narimandoctor@yahoo.com |
| Responsible Party: | NZBakhiet, resident doctor, Assiut University |
| ClinicalTrials.gov Identifier: | NCT03413293 |
| Other Study ID Numbers: |
NBFCIIHCP |
| First Posted: | January 29, 2018 Key Record Dates |
| Last Update Posted: | May 18, 2018 |
| Last Verified: | February 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Infections Communicable Diseases Cross Infection |
Disease Attributes Pathologic Processes Iatrogenic Disease |

