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CompletedNCT07416266Updated Feb 18, 2026

Lower Respiratory Tract Infections Managed in Primary Care in France

An observational study in Lower Respiratory Tract Infections, Community Acquired Pneumonia (CAP) and Acute Bronchitis, sponsored by Hôpital Raymond Poincaré. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-18.

Sponsored by Hôpital Raymond Poincaré · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
230,066
Ages
18 Years and older
Sex
All
01

Study summary

Primary aim:

To describe participant characteristics at the time of the index lower respiratory tract infection (LRTI) episode in adults managed in primary care in France, using anonymized electronic health records from routine clinical practice between January 2015 and December 2024.

Secondary aims:

To describe and quantify patterns of antibiotic prescribing (rate, type, and duration of treatment) and short-term outcomes, including LRTI-related reconsultations and severe complications within 30 days after the index consultation.

The overall objective is to better characterize real-world management and outcomes of lower respiratory tract infections in primary care and to identify potential areas for improving quality of care and optimizing antibiotic stewardship.

Read the detailed description

Lower respiratory tract infections are a frequent reason for consultation and antibiotic prescribing in primary care. However, nationally representative data describing real-world management in routine practice remain limited in France.

This nationwide retrospective observational study uses anonymized electronic health records from the THIN® France database, a large primary care data warehouse collecting routinely recorded clinical data from general practitioners. The study includes adults aged 18 years and older with a recorded episode of community-acquired lower respiratory tract infection between January 2015 and December 2024.

Each participant contributes a single index episode and is followed for 30 days to assess short-term outcomes. The study period allows the evaluation of management practices over a 10-year timeframe in routine ambulatory care.

The main objective is to describe patients characteristics and real-world management of lower respiratory tract infections in primary care, with a focus on patterns of care, treatment strategies, and short-term outcomes. This study is based exclusively on previously collected anonymized data and does not involve any intervention or change in patient care.

By providing a large-scale overview of routine practice, the study aims to improve understanding of current management approaches and identify potential areas for optimizing antibiotic use in primary care.

02

Conditions studied

  • Lower Respiratory Tract Infections
  • Community Acquired Pneumonia (CAP)
  • Acute Bronchitis
  • Acute Exacerbation Chronic Obstructive Pulmonary Disease
  • Influenza

Keywords

  • Primary Care
  • Antimicrobial Stewardship
  • Electronic Health Records
03

In context

Community-Acquired Pneumonia

324 studies on the registry are indexed under Community-Acquired Pneumonia; 77 are open to participants now.

This study's enrollment of 230,066 is above the median of 650 across 111 observational studies indexed under Community-Acquired Pneumonia.

Browse Community-Acquired Pneumonia studies →

Lead sponsor

Hôpital Raymond Poincaré is the lead sponsor of 4 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients (≥18 years) with a recorded episode of community-acquired lower respiratory tract infection (LRTI) in French primary care between January 1, 2015 and December 31, 2024, identified from anonymized electronic health records in the THIN France database. Patients were required to have at least 12 months of prior medical history before the index episode.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥18 years
  • Recorded diagnosis of community-acquired lower respiratory tract infection in primary care between Jan 1, 2015 and Dec 31, 2024
  • At least 12 months of medical history available before the index consultation

Exclusion criteria

Exclusion Criteria:

  • Age \<18 years
  • Less than 12 months of medical data before index date
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
230,066 participants (actual)
Patient registry
No

Groups and cohorts

  • Antibiotic-Treated LRTI

    Adults with a recorded community-acquired lower respiratory tract infection (LRTI) in primary care in France between January 2015 and December 2024 whose index episode was associated with an antibiotic prescription during routine care. No intervention was assigned by the study.

  • Non-Antibiotic-Treated LRTI

    Adults with a recorded community-acquired lower respiratory tract infection (LRTI) in primary care in France between January 2015 and December 2024 whose index episode was not associated with an antibiotic prescription during routine care. No intervention was assigned by the study.

06

What researchers measure

Primary outcomes

  1. Participant Characteristics at Index LRTI Episode

    Descriptive summary of participant characteristics at the index lower respiratory tract infection episode, including age, sex, body mass index, smoking status, alcohol use, comorbidities, and vaccination status, overall and by antibiotic exposure group.

    Time frame: Index consultation

Secondary outcomes

  1. Antibiotic Prescribing Rate

    Proportion of participants with an antibiotic prescription at the index episode, stratified on LRTI type

    Time frame: Index consultation

  2. Type of Antibiotics Prescribed for Antibiotic-treated LRTIs

    Distribution of antibiotic classes prescribed at the index episode.

    Time frame: Index consultation

  3. Duration of Antibiotic Treatment for Antiobiotic-treated LRTIs

    Duration of antibiotic treatment prescribed for the index episode.

    Time frame: Index consultation

  4. 30-Day LRTI-Related Reconsultation Rate

    Proportion of participants with a follow-up consultation related to LRTI within 30 days.

    Time frame: 30 days

  5. 30-Day Severe Complication Rate After LRTI

    Occurrence of Sepsis/septic shock, Pleural effusion, Lung abscess, Acute respiratory distress syndrome (ARDS) within 30 days after the index episode.

    Time frame: 30 days

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Individual participant data come from an anonymized database with legal and contractual restrictions.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2015 to primary completion in Dec 2024, 119 months.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 10, 2026
First posted
Feb 18, 2026
StartActual
Jan 1, 2015
Primary completionActual
Dec 31, 2024
CompletionActual
Jan 9, 2026
Last update
Feb 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07416266
Lead sponsor
Hôpital Raymond Poincaré
Collaborators
Versailles Saint-Quentin-en-Yvelines University, University of Lausanne Hospitals, Clinityx by Gers Data
Responsible party
Sponsor
First posted
Feb 18, 2026
Start date
Jan 1, 2015
Primary completion
Dec 31, 2024
Completion
Jan 9, 2026
Last update
Feb 18, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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