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NCT06729931Completed

Quantitative C-Reactive Protein for Differentiating Tuberculous and Malignant Pleural Effusion: a Cross-Sectional Study

Quantitative C-Reactive Protein for Differentiation Between Tuberculous and Malignant Pleural Effusion: an Institutional Cross-Sectional Study

Source: ClinicalTrials.gov · Last updated 12 Dec 2024

Brief summary (registry, in English)

The goal of this observational study is to evaluate the role of pleural fluid Quantitative C-Reactive Protein (Q-CRP) levels in distinguishing between tuberculous and malignant pleural effusion in adult patients with lymphocytic exudative pleural effusion. The main questions it aims to answer are: Is pleural fluid Q-CRP significantly higher in tuberculous pleural effusion compared to malignant pleural effusion? What is the optimal cutoff value of pleural fluid Q-CRP to differentiate between these conditions? Participants will: Undergo diagnostic procedures such as pleural fluid analysis, including ADA and cytology. Provide pleural fluid samples for Q-CRP measurement. Have additional diagnostic imaging or biopsies if clinically indicated. Researchers will compare Q-CRP levels between the tuberculous pleural effusion group and the malignant pleural effusion group to determine its diagnostic accuracy, including sensitivity, specificity, and predictive value.

Status (registry)
Completed
Study type
Observational
Enrollment
81 (actual)
First submitted
7 Dec 2024
Start date
1 Nov 2022
Primary completion date
1 Nov 2023
Lead sponsor
Maharajgunj Medical Campus
NCT number
NCT06729931

What you commit to

  • Study type: Observational
  • Participants enrolled: 81
  • From 1 Nov 2022 to the primary completion date, 1 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Non-tuberculous and non-malignant lymphocytic exudative pleural effusions identified during diagnostic evaluation.

Other

  • Patients who refuse to provide consent for study participation.
  • Patients requiring biopsy under general anesthesia but found unfit for the procedure.

Who the study is looking for

  • Adults aged 18 years and older.
  • Patients presenting with lymphocytic exudative pleural effusion confirmed by Light's criteria.
  • Lymphocyte predominance in pleural fluid (≥ 50% of differential count).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institute of Medicine, Maharajgunj
Coordinator of this site? Confirm its status
KathmanduNepalUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.