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.
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.
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
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.
- Conditions
- Pleural Infection
- 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 group | Role | What they receive |
|---|---|---|
| Pleural infection | Patients with pleural infection Receives: Diagnostic Test: PRISM PCR panel; Diagnostic Test: Conventional bacterial culture | |
| Non-pleural infection | Patients 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.
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)
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
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.
- First posted22 Jul 2025
- Study start1 Jan 2026 (estimated)
- Primary completion31 Dec 2027 (estimated)
- Study completion30 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pleural InfectionStudies of the same condition, open and under way.
- More trials run by Chinese University of Hong KongThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Chinese University of Hong Kong
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ka Pang Chan, Chinese University of Hong Kong
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
Study at a glance
From the registry record, last updated by the sponsor on 22 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Diagnostic Utility of Pleural Infection-specific Multiplex PCR Panel to Identify Causative Microorganisms in Pleural Infection
- ClinicalTrials.gov ID
- NCT07077096
- Acronym / sponsor ID
- PRISM / PRISM
- Conditions
- Pleural Infection
- Keywords
- Parapneumonic effusion, Pleural effusion, Empyema
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 800 participants (estimated)
- Lead sponsor
- Chinese University of Hong KongUniversity, hospital or other
- Study start
- 1 Jan 2026 (estimated)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 30 Jun 2028 (estimated)
- First posted
- 22 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Pleural infection | – | Diagnostic Test: PRISM PCR panel, Diagnostic Test: Conventional bacterial culturePatients with pleural infection |
| Non-pleural infection | – | Diagnostic Test: PRISM PCR panel, Diagnostic Test: Conventional bacterial culturePatients without pleural infection |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (2 listed)
- Patients hospitalized for new-onset pleural effusion requiring thoracentesis
- Aged 18 years old or above
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PRISM PCR panelComparing the diagnostic accuracy between conventional bacterial culture and multiplex PCR on diagnosing pleural infection | Diagnostic test | Non-pleural infection, Pleural infection |
| Conventional bacterial cultureComparing the diagnostic accuracy between conventional bacterial culture and multiplex PCR on diagnosing pleural infection | Diagnostic test | Non-pleural infection, Pleural infection |
Primary outcome
Diagnostic sensitivity and specificity of the PRISM PCR panel
Time frame: 24 months
The diagnostic performance (sensitivity and specificity ) of the PRISM PCR panel and conventional bacterial culture in diagnosing pleural infection
2 secondary outcomes
the effect of antibiotic on the diagnostic sensitivity and specificity of PRISM PCR panel
Time frame: 24 months
the effect of pleural fluid pH on the diagnostic sensitivity and specificity of PRISM PCR panel
Time frame: 24 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jul 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
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.