Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT06097117 |
Other study ID # |
role of multiplex PCR in CAP |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
November 1, 2023 |
Est. completion date |
December 1, 2024 |
Study information
Verified date |
October 2023 |
Source |
Assiut University |
Contact |
Asmaa Saleh Mousa, resident physician |
Phone |
01149227845 |
Email |
asmaa241.saleh[@]gmail.com |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
1. role of multiplex PCR in early identifying bacteria in patients with lower respiratory
tract infection.
2. effect of early starting targeted antibiotics on outcome
Description:
Pneumonia remains a worldwide health problem with a high rate of morbidity and mortality.
Identification of microbial pathogens which cause pneumonia is an important area for optimum
clinical management of pneumonia patients and is a big challenge for conventional
microbiological methods. The development and implementation of molecular diagnostic tests for
pneumonia has been a major advance in the microbiological diagnosis of respiratory pathogens
in recent years. Targeted antibiotic selection and more effective de-escalation and improved
stewardship for pneumonia patients.
PCR is a simple, yet elegant, enzymatic assay, which allows for the amplification of a
specific DNA fragment from a complex pool of DNA.. Only trace amounts of DNA are needed for
PCR to generate enough copies to be analyzed using conventional laboratory methods. For this
reason, PCR is a sensitive assay.
Each PCR assay requires the presence of template DNA, primers, nucleotides, and DNA
polymerase .The DNA polymerase is the key enzyme that links individual nucleotides together
to form the PCR product. The nucleotides include the four bases - adenine, thymine, cytosine,
and guanine (A, T, C, G) - that are found in DNA. These act as the building blocks that are
used by the DNA polymerase to create the resultant PCR product. The primers in the reaction
specify the exact DNA product to be amplified. The primers are short DNA fragments with a
defined sequence complementary to the target DNA that is to be detected and amplified. These
serve as an extension point for the DNA polymerase to build on.There are multiple advantages
to PCR. First, it is a simple technique to understand and to use, a nd it produces results
rapidly. It is a highly sensitive technique with the potential to produce millions to
billions of copies of a specific product for sequencing, cloning, and analysis. Although PCR
is a valuable technique, it does have limitations. Because PCR is a highly sensitive
technique, any form of contamination of the sample by even trace amounts of DNA can produce
misleading results . In addition, in order to design primers for PCR, some prior sequence
data is needed. Therefore, PCR can only be used to identify the presence or absence of a
known pathogen or gene