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CompletedNCT04158804ProSAVEUpdated Mar 20, 2025Results posted

PROcalcitonin Impact on Antibiotic Reduction, adverSe Events and AVoidable healthcarE Costs (ProSAVE): A RCT

An interventional study of procalcitonin in Pneumonia, Bacterial, sponsored by Massachusetts General Hospital. Completed at 6 sites in United States. Open to participants aged 18 Years to 110 Years. Per ClinicalTrials.gov, last updated 2025-03-20.

Sponsored by Massachusetts General Hospital · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
700
Allocation
Randomized
Ages
18 Years to 110 Years
Sex
All
01

Study summary

Trials comparing PCT-guided antibiotic algorithms to standard management show a significant reduction in antibiotic exposure without an increase in mortality or treatment failure. Despite this strong evidence from multiple studies a recent prospective multicentric interventional trial in the US fell short of demonstrating antibiotic reductions by PCT-guided antibiotic management. Amongst other limitations the authors of that study concluded that successful implementation of PCT may require closer educational oversight. As such, this study will compare effectiveness and safety of antibiotic prescription guided by a PCT-algorithm via a Stewardship Team over standard guidelines in hospitalized adult patients with suspected or confirmed LRTI (including sepsis with respiratory focus).

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Conditions studied

  • Pneumonia, Bacterial

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03

In context

Pneumonia, Bacterial

156 studies on the registry are indexed under Pneumonia, Bacterial; 19 are open to participants now.

This study's enrollment of 700 is above the median of 121 across 105 interventional studies indexed under Pneumonia, Bacterial.

Browse Pneumonia, Bacterial studies →

Lead sponsor

Massachusetts General Hospital is the lead sponsor of 2,536 studies on the registry; 446 are open to participants now.

Of its 214 completed or terminated interventional studies of FDA-regulated products, 161 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 110 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Hospitalized adult patients ≥ 18 years of age
  • Suspected or confirmed pneumonia \<28 days at time of admission to the hospital (ED) who are prescribed antibiotics
  • Minimum of 2 (two) blood samples available for PCT value assessment within 24 hours of hospitalization

Exclusion criteria

Exclusion Criteria:

  • Patient has tested positive for SARS-CoV-2
  • Non-hospitalized patients
  • Patients admitted to home health
  • Major surgeries, defined as any procedure in which an incision is made with the exception of superficial procedures (eyes, cornea, skin, dental procedures), organs removed, or normal anatomy altered (e.g. open thoracic, abdominal and/or major orthopedic surgery), in the past 1 month or expected surgical procedure or patient receiving antibiotics for surgical prophylaxis
  • Active metastatic cancer or neuroendocrine tumor or liquid tumor and/or on check point inhibitors within 3 months or has signs of mucositis (e.g. mouth lesions or intestinal bleeding)
  • Known pregnancy
  • Primary and acquired cell-mediated immune deficiency (HIV with CD4 \<350 cells/mm³; receipt of systemic chemotherapy and/or biologics in the past 3 months for reasons other than malignancy)
  • Infection where long course antibiotics are the standard of care(>2 weeks) other than anti-inflammatory reasons.
  • Neutropenia (\<1,500 ANC)
  • Concomitant non-pulmonary bacterial infection that requires antibiotic therapy based on an active medical team decision
  • Antibiotics given for non-infectious indications (e.g. rifaximin for hepatic encephalopathy)
  • Patients with cystic fibrosis
  • Patients receiving dialysis
  • Patients with solid organ transplant, bone marrow transplant or stem cell transplant recipient
  • ST elevation myocardial infarction
  • Prior enrollment into this study within 30 days
  • Patient experiencing major trauma defined as any injury that could cause prolonged disability and/or an Injury Severity Score >15, and/or burns or patient under extracorporeal circulation confirmed by a second research staff member.
  • Patient with acute viral hepatitis and/or decompensated severe liver cirrhosis (Child-Pugh Class C).
  • Patient with prolonged or severe cardiogenic shock, defined as decreased cardiac output leading to end organ injury (e.g. severe hypotension or AKI or oliguria or altered mental status or cool extremities or respiratory distress AND evidence of metabolic acidosis on lab testing)
  • Patient with pancreatitis, chemical pneumonitis or heat stroke
  • Active infection with invasive fungal pathogen (e.g. candidiasis, aspergillosis) or plasmodium falciparum malaria or mycobacteria
  • Patient under treatment with OKT3 antibodies, OK-432, interleukins, TNF-alpha and other drugs stimulating the release of pro-inflammatory cytokines or resulting in anaphylaxis.
  • Patient is under hospice care
  • Patient with ventilator associated pneumonia
  • Patients with untreated, active, and symptomatic autoimmune disease
  • Patients with empyema, abscess, or cavitary/necrotizing pneumonia
  • Patients actively enrolled in other clinical trial involving immunomodulatory therapy
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
700 participants (actual)

Study arms

  • Experimental
    Procalcitonin algorithm+stewardship team

    antibiotic prescription guided by PCT values

    Diagnostic Test: procalcitonin

  • No intervention
    standard group

    standard of care guided by current guidelines

Interventions

  • Diagnostic testprocalcitonin

    accuracy of procalcitonin as a diagnostic marker in guiding antibiotic therapy in patients with a lower respiratory tract infection

06

What researchers measure

Primary outcomes

  1. Short Treatment of Pneumonia

    Proportion of patients with short treatment of pneumonia with antibiotics (less than 4 days, "shortABx")

    Time frame: 30 days

Secondary outcomes

  1. Composite Safety Adverse Event Rate

    Composite endpoints include: all-cause in-hospital mortality, all-cause mortality after discharge (as available), hospital readmission, septic shock (vasopressor use for \> 1 hour), mechanical ventilation (via endotracheal tube), required dialysis, lung abscess/empyema/cavitation/necrotizing pneumonia

    Time frame: 30 days

  2. Antibiotic Exposure at Discharge

    Duration of antibiotics prescribed at discharge

    Time frame: 30 days

  3. Days of Therapy Per 1000 Patient Days

    Days of therapy per 1000 patient days (inclusive of antibiotics prescribed at discharge)

    Time frame: 30 days

  4. Length of Stay

    Length of stay in hospital

    Time frame: 30 days

  5. ICU Admissions

    Number of Participants Admitted to the ICU

    Time frame: 30 days

Other outcomes

  1. Clostridium Difficile Infection (CDI)

    Treatment or readmission for CDI until day 30 after enrollment

    Time frame: 30 days

  2. Healthcare Economic Endpoints

    Costs associated with primary hospitalization, readmission for CDI, and loss of function

    Time frame: 30 days

07

Results

Posted Mar 20, 2025

Participant flow

Participant flow — Overall Study
MilestoneStandard of Care (SOC)PCT/ASP
Started357343
Completed357343
Not completed00

Outcome measures

PrimaryShort Treatment of Pneumonia

Proportion of patients with short treatment of pneumonia with antibiotics (less than 4 days, "shortABx")

Time frame:
30 days
Reported as:
Count of participants · Participants
Short Treatment of Pneumonia
ParticipantsStandard of Care (SOC)PCT/ASP
Short Treatment of Pneumonia4787
SecondaryComposite Safety Adverse Event Rate

Composite endpoints include: all-cause in-hospital mortality, all-cause mortality after discharge (as available), hospital readmission, septic shock (vasopressor use for \> 1 hour), mechanical ventilation (via endotracheal tube), required dialysis, lung abscess/empyema/cavitation/necrotizing pneumonia

Time frame:
30 days
Reported as:
Count of participants · Participants
Composite Safety Adverse Event Rate
ParticipantsStandard of Care (SOC)PCT/ASP
Composite Safety Adverse Event Rate7290
SecondaryAntibiotic Exposure at Discharge

Duration of antibiotics prescribed at discharge

Time frame:
30 days
Reported as:
Median · days
Antibiotic Exposure at Discharge
daysStandard of Care (SOC)PCT/ASP
Antibiotic Exposure at Discharge0 (0 to 4)0 (0 to 2)
SecondaryDays of Therapy Per 1000 Patient Days

Days of therapy per 1000 patient days (inclusive of antibiotics prescribed at discharge)

Time frame:
30 days
Reported as:
Median · Days of Therapy Per 1000 Patient Days
Days of Therapy Per 1000 Patient Days
Days of Therapy Per 1000 Patient DaysStandard of Care (SOC)PCT/ASP
Days of Therapy Per 1000 Patient Days1.25 (0.78 to 2.67)1.14 (0.67 to 2)
SecondaryLength of Stay

Length of stay in hospital

Time frame:
30 days
Reported as:
Median · days
Length of Stay
daysStandard of Care (SOC)PCT/ASP
Length of Stay4 (2 to 7)4 (3 to 7)
SecondaryICU Admissions

Number of Participants Admitted to the ICU

Time frame:
30 days
Reported as:
Count of participants · Participants
ICU Admissions
ParticipantsStandard of Care (SOC)PCT/ASP
ICU Admissions4349
Other pre-specifiedClostridium Difficile Infection (CDI)

Treatment or readmission for CDI until day 30 after enrollment

Time frame:
30 days

Results for this outcome have not been posted.

Other pre-specifiedHealthcare Economic Endpoints

Costs associated with primary hospitalization, readmission for CDI, and loss of function

Time frame:
30 days

Results for this outcome have not been posted.

Adverse events

Collected over Adverse event data was collected starting at enrollment day until 30 days after enrollment.. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Standard of Care (SOC)19/357 (5.3%)76/357 (21.3%)0/357 (0%)
PCT/ASP17/343 (5%)81/343 (23.6%)0/343 (0%)
Most frequent serious events
Most frequent serious events
EventStandard of Care (SOC)PCT/ASP
ReadmissionGeneral disorders47/35757/343
DeathGeneral disorders19/35717/343
Septic ShockInfections and infestations11/35713/343
Mechanical VentilationRespiratory, thoracic and mediastinal disorders5/35713/343
EmpyemaInfections and infestations3/3576/343
DialysisRenal and urinary disorders3/3570/343

Baseline characteristics

Age, Continuous
Age, Continuous(years)Standard of Care (SOC)PCT/ASPTotal
Median73 (61 to 84)71 (60 to 81)72 (61 to 82)
Sex: Female, Male
Sex: Female, Male(Participants)Standard of Care (SOC)PCT/ASPTotal
Female166164330
Male191179370
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Standard of Care (SOC)PCT/ASPTotal
Hispanic or Latino432972
Not Hispanic or Latino305303608
Unknown or Not Reported91120
Pneumonia Type
Pneumonia Type(Participants)Standard of Care (SOC)PCT/ASPTotal
CAP (community-acquired pneumonia)205196401
HCAP (healthcare-associated pneumonia)101525
Aspiration8982171
Other5350103
Pneumonia Severity Index (PSI)
Pneumonia Severity Index (PSI)(Participants)Standard of Care (SOC)PCT/ASPTotal
Class I (lowest severity)141630
Class II454489
Class III7864142
Class IV144156300
Class V (highest severity)7663139
08

Study locations

6 sites
  • Charlotte Hungerford Hospital
    Torrington, Connecticut 06790, United States
  • Grady Memorial Hospital
    Atlanta, Georgia 30303, United States
  • Massachusetts General Hospital
    Boston, Massachusetts 02114, United States
  • Martha's Vineyard Hospital
    Oak Bluffs, Massachusetts 02557, United States
  • North Shore Medical Center
    Salem, Massachusetts 01970, United States
  • Texas Health Harris Methodist Hospital
    Fort Worth, Texas 76104, United States
09

References and documents

Study documents

  • Study protocol · Jun 8, 2023
  • Statistical analysis plan · Jun 12, 2023

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT04158804
Lead sponsor
Massachusetts General Hospital
Collaborators
BRAHMS GmbH, Thermo Fisher Scientific, Inc
Responsible party
Michael K. Mansour (Assistant Professor of Medicine, Massachusetts General Hospital) — Principal investigator
First posted
Nov 12, 2019
Start date
May 28, 2020
Primary completion
Jun 17, 2023
Completion
Jun 17, 2023
Results posted
Mar 20, 2025
Last update
Mar 20, 2025

Study contacts

Michael K Mansour, MD, PhD
principal investigator · Massachusetts General Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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