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Cancer Ratio,Pleural Fluid Adenosine Deaminase,Lactate Dehydrogenase, interferonY, Tumor Necrosis Factor,and Interleukins{2,12,18}for Differentiation Between Malignant and Non Malignant Pleural Effusion

Cancer Ratio,Pleural Fluid Adenosine Deaminase,Lactate Dehydrogenase, interferonY, Tumor Necrosis Factor,and Interleukins{2,12,18}for Differentiation Between Malignant and Non Malignant Pleural Effusion

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05693727
Enrollment
100
Registered
2023-01-23
Start date
2023-09-01
Completion date
2027-09-01
Last updated
2023-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pleural Effusion, Malignant

Brief summary

To evaluate the ability of cancer ratio and pleural fluid markers to discriminate between malignant and non malignant effusion

Detailed description

Pleural effusion is a common clinical entity affecting approximately 1.5 million patients per year in the United States. {3.1}A large number of diseases may be associated with pleural effusion. This includes: * Local conditions affecting the pleura (eg, tuberculous pleurisy, pleural mesothelioma), * Extrapulmonary diseases with secondary pleural involvement (eg, chronic heart failure, liver cirrhosis). To date, differentiation between both types of pleural effusion (exudate and transudate) is the most common initial diagnostic approach for patients with pleural effusion. Exudative effusion is commonly seen in three conditions namely cancer (MPE), tuberculosis (TB) and para pneumonic Although MPE can be diagnosed by simple pleural fluid cytology, this method has significant limitations, including a highly variable sensitivity, ranging from as low as 11.6% to as high as 71%. In contrast to other common causes of pleural effusion such as T.B, no accurate biomarkers of MPE have been established. Several tumor markers were extensively evaluated, including carcinoembryonic antigen, cytokeratin-19 fragments, and cancer antigen 125, but none of them were found sensitive and specific enough to be implemented in routine clinical practice

Interventions

DIAGNOSTIC_TESTpleural markers

Pleural Fluid Adenosine Deaminase,Lactate Dehydrogenase, interferonY, Tumor Necrosis Factor,and Interleukins{2,12,18}

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients (100 cases) with exudative pleural effusion who will be admitted to Department of Chest diseases and Tuberculosis, Assiut University Hospital

Exclusion criteria

* Age ˂ 18 years * Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Differentiate between malignant and non malignant pleural effusion by pleural markersBaselineusing pleural markers

Secondary

MeasureTime frameDescription
Time savingBaselinedecrease the need for invasive maneuvers for diagnosis * decrease length of hospital stay * decrease the development of complications

Contacts

Primary ContactMona Adel Mostafa, Master
maiadel9995@gmail.co01124629683

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026