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Pleural InfectionPRISMNCT07077096

Diagnostic Utility of Pleural Infection-specific Multiplex PCR Panel

An observational study of Pleural Infection, run by Chinese University of Hong Kong at 1 site in Hong Kong.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Pleural effusion is a common cause of hospitalization. Pleural infection ranked third among the pleural effusions requiring hospitalization in the United States. Pleural infection, including complicated parapneumonic effusion and empyema, is associated with a 30-day mortality of 10%. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pleural Infection
What is being tested?
PRISM PCR panel and Conventional bacterial culture
How many people
800 participants
Where
1 siteHong Kong
Study dates
1 Jan 2026to 30 Jun 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with pleural infection will be recruited as positive control. Patients without pleural infection will be recruited as negative control.

Who may be able to join

  • Patients hospitalized for new-onset pleural effusion requiring thoracentesis
  • Aged 18 years old or above

Who cannot join

  • History of tuberculous pleuritis and bacterial pleural infection in the ipsilateral pleural space
  • History of intrapleural therapy (including talc and fibrinolytic) in the ipsilateral pleural space
  • History of surgical decortication or pleurodesis in the ipsilateral pleural space
  • Eczematous or infected cutaneous conditions at the site of planned pleural procedure that may increase the risk of contamination during the procedure
  • Failed to obtain informed consent due to the patient's refusal or cognitive impairment

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ka Pang Chan, MBChB contact

35052211

chankapang@cuhk.edu.hk

Hong Kong1 site
  • Prince of Wales Hospital

    Hong Kong

    Ka Pang Chan, MBChB, 35053396, chankapang@cuhk.edu.hk

    David SC Hui, MD, 852 26323128, dschui@cuhk.edu.hk

Other trials in Hong Kong

About this study

Official title: Diagnostic Utility of Pleural Infection-specific Multiplex PCR Panel to Identify Causative Microorganisms in Pleural Infection

Pleural effusion is a common cause of hospitalization. Pleural infection ranked third among the pleural effusions requiring hospitalization in the United States. Pleural infection, including complicated parapneumonic effusion and empyema, is associated with a 30-day mortality of 10%. Approximately 20-57% of patients with pneumonia have an associated pleural effusion at presentation, of which 5-7% progress to pleural infection. Analyses of several nation-wide healthcare databases in the United States, France and the United Kingdom have showed an increasing incidence of pleural infection in the past decade.

Adequate antibiotic coverage and fluid drainage are the two pillars of treatment for pleural infection. The empirical use of antibiotics should be based on the local spectrum of causative microorganisms and the source of infection. Subsequent targeted antibiotic regimen can be guided by the culture results and sensitivity pattern of the cultured microorganisms. The use of blood culture bottles as the transfer medium can improve the culture positivity from 30-40% to 60%. An explorative study of culturing pleural tissue can increase the microbiological yield from 20% to 45%. Despite these methods, the culture positivity rates are far from 100% although clinical evidence of pleural infection. Peripheral blood cultures may occasionally be the only positive source of culture (12%). Occasionally, complicated malignant pleural effusion (MPE) can mimic pleural infection, by sharing similar biochemical features of high neutrophil counts and lactate dehydrogenase in the pleural fluid. This would subject the patients with MPE to unnecessary prolonged course of antibiotic and delay of chemotherapy. Prolonged course of broad-spectrum antibiotics (BSA) is commonly required for culture-negative pleural infection or MPE with complicated features, but it could lead to various antibiotic-related adverse events, including kidney and liver injuries, opportunistic infections (e.g. Clostridioides difficile colitis). These are clinical unmet needs of identifying causative microorganisms in pleural infection.

Read more

The application of multiplex bacterial polymerase chain reaction (PCR) panel has transformed the care of patients with respiratory infection. Incorporating multiplex bacterial PCR test of bronchoalveolar lavage in hospitalized patients with pneumonia at risk of Gram-negative bacterial infection can significantly shorten the duration of inappropriate antibiotic therapy. For patients with suspected lower respiratory tract infection, this platform allows early antibiotic adjustment (faster antibiotic escalations for Gram-negative or Gram-positive bacteria, and faster antibiotic de-escalations directed at Gram-positive bacteria). The use of multiplex PCR panel designed for pneumonia has been applied to patients with parapneumonic effusion with successful identification of non-culturable microorganism. However, the use of pneumonia multiplex PCR panels has not been fully validated in the clinical management of pleural infection. More importantly, these panels only detect common microorganisms included on their panels specifically designed for pneumonia. Therefore, a dedicated pleural infection-specific multiplex (PRISM) PCR panel is required to enhance the identification for microorganisms in patients presenting with pleural infection.

A syndromic real-time PCR panel for diagnosing community-acquired pleural infection has been established by a Norway group, with its components constructed based on the next-generation sequencing results using prior pleural infection samples. Their panel showed a higher diagnostic sensitivity than that of conventional culture-based methods. For bacterial species included in the PCR panel, it had a sensitivity of 99.5%. However, it lacks clinical performance data and may not be applicable in the South-East Asian region as the microbiological spectrum of pleural infection differs geographically, with pneumococci and viridans streptococci the most commonly reported isolates from tropical and temperate regions, respectively. Therefore, a PRISM PCR panel dedicated for South-East Asian population is highly warranted. The investigators has developed a PRISM PCR panel dedicated for local population. The investigators hypothesize that this new PRISM PCR panel has higher diagnostic sensitivity than conventional culture-based methods in identifying causative microorganisms in prospectively collected real-world pleural fluid specimens.

Being tested
PRISM PCR panel, Conventional bacterial culture
Keywords
Parapneumonic effusion, Pleural effusion, Empyema
Medical subject headings
Pleural Effusion, Empyema

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PRISM PCR panelDiagnostic test

    Comparing the diagnostic accuracy between conventional bacterial culture and multiplex PCR on diagnosing pleural infection

  • Conventional bacterial cultureDiagnostic test

    Comparing the diagnostic accuracy between conventional bacterial culture and multiplex PCR on diagnosing pleural infection

Study groups in NCT07077096
Study groupRoleWhat they receive
Pleural infectionPatients with pleural infection
Receives: Diagnostic Test: PRISM PCR panel; Diagnostic Test: Conventional bacterial culture
Non-pleural infectionPatients without pleural infection
Receives: Diagnostic Test: PRISM PCR panel; Diagnostic Test: Conventional bacterial culture

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diagnostic sensitivity and specificity of the PRISM PCR panel

    The diagnostic performance (sensitivity and specificity ) of the PRISM PCR panel and conventional bacterial culture in diagnosing pleural infection

    Measured: 24 months

Secondary outcomes (2)
  1. the effect of antibiotic on the diagnostic sensitivity and specificity of PRISM PCR panel

    Evaluation of the effect of time difference between intiation of antibiotic and pleural fluid aspiration on the diagnostic accuracy (sensitivity and specificity) of PRISM PCR panel in diagnosing pleural infection

    Measured: 24 months

  2. the effect of pleural fluid pH on the diagnostic sensitivity and specificity of PRISM PCR panel

    Evaluation of the effect of pleural fluid pH on the diagnostic accuracy (sensitivity and specificity) of PRISM PCR panel in diagnosing pleural infection

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2025
  2. Study start1 Jan 2026 (estimated)
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion30 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
800 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07077096
Sponsor's protocol ID
PRISM
Acronym
PRISM
Status last verified
Jul 2025
First submitted
3 Jul 2025
Last updated
22 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Pleural Infection, run by Chinese University of Hong Kong at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 22 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ka Pang Chan, MBChB (35052211, chankapang@cuhk.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diagnostic sensitivity and specificity of the PRISM PCR panel (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2025.

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