The Procalcitonin Guided Antibiotics in Respiratory Infections in General Practice (PARI)
Primary Purpose
Acute Respiratory Tract Infection
Status
Withdrawn
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Procalcitonin
Sponsored by
About this trial
This is an interventional diagnostic trial for Acute Respiratory Tract Infection focused on measuring primary care, acute respiratory tract infection, Procalcitonin, general practice, Antibiotic use
Eligibility Criteria
Inclusion Criteria:
- Age above 18 years
- Able to read and understand patient information about the PARI trial and willing to give written informed consent prior to enrollment
- Acute cough e.g. less than 2 weeks probable acute upper or lower respiratory tract infection (pharyngitis, tonsillitis, otitis media, sinusitis, exacerbations of asthma or Chronic Obstructive Pulmonary Disease (COPD), bronchitis or pneumonia)
- C-Reactive Protein >20 mg/m
Exclusion Criteria:
- Symptoms present for more than 2 weeks
- Verified immunodeficiency or presently neutropenic (neutrophile granulocytes ≤0,5 x 109/L within the last 7 days)
- Severe liver failure
- Severe kidney failure including dialysis
- Sore throat and positive test for Group A streptococcus
- Prior antibiotic exposure last 14 days up to inclusion
- Need for acute admission to hospital
- Pregnancy or breastfeeding
Sites / Locations
- Lægerne Finne, Riise og Aabenhus
- Amagercentrets læger
- Mit Lægehus
- Haslev Lægecenter
- Næstved Lægecenter
- Rønnede lægehus
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Procalcitonin in addition to usual care
Usual care
Arm Description
Procalcitonin values will be disclosed to the attending physician and assist in antibiotic guidance in addition to usual care
Usual best standard care. No procalcitonin values disclosed to attending physician .
Outcomes
Primary Outcome Measures
Duration of illness and symptoms from acute respiratory tract infections.
The patient reported primary outcome will be assessed as number of days to a patient's daily activities (work or recreation) are no longer restricted by symptoms from a respiratory tract infection.The non-inferiority margin between the intervention and control group is set at a one day difference. The recovery measure will be the specific day indicated by the participants using the validated Acute Respiratory Tract Infections Questionaire (ARTIQ).
Secondary Outcome Measures
Antibiotic treatments
Number of participants in each trial arm exposed to antibiotic treatment at index consultation (day 1) and within 30 days
Side effects from antibiotic treatment
Number of participants in each trial arm with side effects from antibiotic treatment
re-consultations
Number of participants in each trial arm with re-consultations
Severe adverse effects
Number of participants in each trial arm admitted to hospitalization (including diagnosis and mortality)
Biomarker levels
Characterisation of biomarker (C-Reactive Protein and Procalcionin) levels at index consultation.
Full Information
NCT ID
NCT04216277
First Posted
December 12, 2019
Last Updated
March 23, 2023
Sponsor
Chronic Obstructive Pulmonary Disease Trial Network, Denmark
Collaborators
Research Unit Of General Practice, Copenhagen, Department of Public Health, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT04216277
Brief Title
The Procalcitonin Guided Antibiotics in Respiratory Infections in General Practice
Acronym
PARI
Official Title
The Procalcitonin Guided Antibiotics in Respiratory Infections in General Practice
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Withdrawn
Why Stopped
the poc test was withdrawn by manufacturer
Study Start Date
February 27, 2020 (Actual)
Primary Completion Date
August 1, 2022 (Actual)
Study Completion Date
August 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chronic Obstructive Pulmonary Disease Trial Network, Denmark
Collaborators
Research Unit Of General Practice, Copenhagen, Department of Public Health, Denmark
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Antimicrobial resistance rates have reached alarming levels and the Worlds Health Organisation (WHO) states it constitutes a serious public health concern by threatening one of the most effective and mortality lowering interventions in modern medicine. Part of the solution to this problem includes minimizing overuse of antibiotics. But clinical signs alone are often not reliable to guide antibiotic treatment decisions and additional tests may be warranted to assist the doctor. Such tests include point-of-care biomarkers of infection like C-reactive protein (CRP) and procalcitonin (PCT). Targeting antibiotic use to the few patients with a high probability of benefit and withholding in the many with non-serious respiratory infection is a promising strategy and readily implemented in clinical practice.
The Procalcitonin guided Antibiotics in Respiratory Infections (PARI) study will assess the effect of a novel point-of-care PCT guided antibiotic stewardship in acute respiratory tract infections in general practice.
The overall aim of the PARI study is to reduce antibiotic use in patients with acute respiratory tract infections by targeting antibiotic treatment only to patients with a suspected bacterial etiology and thus likely to benefit from antibiotic therapy.
The main research questions are:
Does the addition of a point-of-care Procalcitonin test to standard care reduce antibiotic use in primary care? Is the intervention safe for the patients? The PARI study is a pragmatic two-arm (intervention and control (standard care) open randomized non-inferiority trial (up to 1 day difference in recovery) in general practice.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Tract Infection
Keywords
primary care, acute respiratory tract infection, Procalcitonin, general practice, Antibiotic use
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Procalcitonin will be measured on all participants but none of the participants will be informed about the results of the procalcitonin value or the randomisation and thus remain unaware of allocated group status (intervention or control).
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Procalcitonin in addition to usual care
Arm Type
Experimental
Arm Description
Procalcitonin values will be disclosed to the attending physician and assist in antibiotic guidance in addition to usual care
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Usual best standard care. No procalcitonin values disclosed to attending physician .
Intervention Type
Diagnostic Test
Intervention Name(s)
Procalcitonin
Intervention Description
In addition to usual care diagnostic and handling of acute respiratory tract infections in general practice to attending physician in the intervention arm has access to antibiotic stewardship by a procalcitonin point-of-care test. The following criteria for initiating og withholding antibiotics will be used.
Antibiotics treatment is recommended with Procalcitonin levels above 0.25 ng/ml
Antibiotic treatment is discouraged if Procalcitonin levels are below 0.25 ng/ml
Primary Outcome Measure Information:
Title
Duration of illness and symptoms from acute respiratory tract infections.
Description
The patient reported primary outcome will be assessed as number of days to a patient's daily activities (work or recreation) are no longer restricted by symptoms from a respiratory tract infection.The non-inferiority margin between the intervention and control group is set at a one day difference. The recovery measure will be the specific day indicated by the participants using the validated Acute Respiratory Tract Infections Questionaire (ARTIQ).
Time Frame
up to 14 days
Secondary Outcome Measure Information:
Title
Antibiotic treatments
Description
Number of participants in each trial arm exposed to antibiotic treatment at index consultation (day 1) and within 30 days
Time Frame
1, 14 and 30 days
Title
Side effects from antibiotic treatment
Description
Number of participants in each trial arm with side effects from antibiotic treatment
Time Frame
14 days
Title
re-consultations
Description
Number of participants in each trial arm with re-consultations
Time Frame
30 days
Title
Severe adverse effects
Description
Number of participants in each trial arm admitted to hospitalization (including diagnosis and mortality)
Time Frame
30 days
Title
Biomarker levels
Description
Characterisation of biomarker (C-Reactive Protein and Procalcionin) levels at index consultation.
Time Frame
day 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age above 18 years
Able to read and understand patient information about the PARI trial and willing to give written informed consent prior to enrollment
Acute cough e.g. less than 2 weeks probable acute upper or lower respiratory tract infection (pharyngitis, tonsillitis, otitis media, sinusitis, exacerbations of asthma or Chronic Obstructive Pulmonary Disease (COPD), bronchitis or pneumonia)
C-Reactive Protein >20 mg/m
Exclusion Criteria:
Symptoms present for more than 2 weeks
Verified immunodeficiency or presently neutropenic (neutrophile granulocytes ≤0,5 x 109/L within the last 7 days)
Severe liver failure
Severe kidney failure including dialysis
Sore throat and positive test for Group A streptococcus
Prior antibiotic exposure last 14 days up to inclusion
Need for acute admission to hospital
Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Bjerrum, PhD
Organizational Affiliation
Department of Public Health, Copenhagen University, Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Lægerne Finne, Riise og Aabenhus
City
Copenhagen
ZIP/Postal Code
1620
Country
Denmark
Facility Name
Amagercentrets læger
City
Copenhagen
ZIP/Postal Code
2300
Country
Denmark
Facility Name
Mit Lægehus
City
Copenhagen
ZIP/Postal Code
2610
Country
Denmark
Facility Name
Haslev Lægecenter
City
Haslev
ZIP/Postal Code
4690
Country
Denmark
Facility Name
Næstved Lægecenter
City
Næstved
ZIP/Postal Code
4700
Country
Denmark
Facility Name
Rønnede lægehus
City
Rønnede
ZIP/Postal Code
4683
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
work in progress
IPD Sharing Time Frame
Upon publication of study results
Citations:
PubMed Identifier
35279069
Citation
Filipsen N, Bro H, Bjerrum L, Jensen JS, Aabenhus R. The Procalcitonin-guided Antibiotics in Respiratory Infections (PARI) project in general practice - a study protocol. BMC Prim Care. 2022 Mar 12;23(1):43. doi: 10.1186/s12875-022-01646-6.
Results Reference
derived
Learn more about this trial
The Procalcitonin Guided Antibiotics in Respiratory Infections in General Practice
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