Customized Antibiotic Treatment Duration Among Hospitalized Patients With Moderately Severe Community-Acquired Pneumonia

NCT ID: NCT05903352

Last Updated: 2025-03-20

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 328 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-02-05
• Study Completion Date: 2027-05-31

Brief Summary

The primary objective of the study is to evaluate if the efficacy of an experimental strategy on antibiotic treatment duration based on stopping treatment when stability criteria are reached after at least 48 h of treatment, is non-inferior to the efficacy of standard antibiotic duration in CAP patients treated in the hospital setting.

As the secondary objectives, the study aims

• To study if the efficacy of our experimental strategy on antibiotic treatment duration compared to standard of care in CAP patients treated in the hospital setting is non-inferior in terms of:

• Persistence of cure at Day 30 of antibiotic treatment
• All-cause mortality rate on Day 30 of antibiotic treatment
• Patients evolution of pneumonia symptoms and quality of life via 2 scores (CAP score, CAP Sym) at Day 0 of treatment (retrospectively), at stability (Day S), at Day 7 , at Day 15, and at Day 30 of antibiotic treatment.
• To compare between the 2 study arms at Day 30 of antibiotic treatment:

• The duration of antibiotic treatment;
• The length of hospital stay;
• The frequency and severity of adverse events during the 30 days after the start of treatment.
• To explore the impact of reduced antibiotic treatment duration for CAP on the oropharyngeal resistome.

Detailed Description

Recent studies have suggested that community-acquired pneumonia (CAP) can be successfully treated with short-course antibiotic regimen when clinical improvement is rapidly obtained. Even if clinical response is obtained in 3 days in the majority of cases, it can vary widely among patients suggesting "one duration does not fit all". An individualised duration of therapy depending on the patient's response could help to ensure bacterial eradication while avoiding unnecessary antibiotic exposure and thus reduce antibiotic resistance. At present, this strategy has never been tested.

This is a phase III, pragmatic, non-inferiority randomised (1:1) national multicentre trial. Population of study participants will be patients admitted to hospital with suspected CAP and in need for antibiotics.

There is no need to establish a DSMB for this trial. The antibiotic treatments prescribed during this study are treatments used in current practice, with well-known adverse drug reactions. Furthermore, a 3-day treatment duration has already been studied in 2 previous randomized clinical trials, showing its safety for hospitalized CAP.

Statistical analysis:

Statistical inference for non-inferiority will be based on the confidence intervals (CI) of the difference in Day 15 cure proportions [proportion in reference arm - proportion in experimental arm] accounting for randomisation stratification factors (centre and delay from Day 0 to Day S (≤ 3 days or > 3 days).

The inferiority hypothesis will be rejected and non-inferiority will be claimed if the upper bound of the 95%CI of the difference is ≤ 10%.

Secondary efficacy endpoints evaluating the evolution of symptoms will be analysed using either a GMM or a GEE for categorical and continuous variables, respectively.

Other quantitative variables will be compared using the Student t-test (or a non-parametric test if the distribution remains skewed following transformation), while categorical variables will be analysed using either the Chi-squared or the Fisher-exact tests.

All statistical tests will be performed with a level of significance of 5%, except the primary endpoint which be analysed with a 2.5% level of significance.

Conditions

Community-Acquired Pneumonia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Antibiotic treatment

Antibiotic treatment duration left to the physician's judgment (usual practice: total treatment duration between 5 to 10 days according to French guidelines; more than 7 days of treatment should be justified).

Group Type: PLACEBO_COMPARATOR

Continue the antimicrobial treatment

Intervention Type: DRUG

Continue the antimicrobial treatment for a duration predetermined by the investigator (usual practice, at least 5 days of treatment in total).

Interruption of treatment

Interruption of treatment based on the patient reaching all of the following stability criteria (body temperature ≤ 37.8°C; heart rate ≤ 100/min; systolic blood pressure \> 90mmHg; oxygen saturation ≥ 92%; respiratory rate \< 24/min; normal mental status (27)), with a treatment duration no shorter than 48 h.

Group Type: EXPERIMENTAL

Stop antibiotic

Intervention Type: OTHER

Stop the antibiotic treatment on day S (stability criteria reached for 24 h or within 48 hours after the start of antibiotic treatment).

Interventions

Stop antibiotic

Stop the antibiotic treatment on day S (stability criteria reached for 24 h or within 48 hours after the start of antibiotic treatment).

Intervention Type: OTHER

Continue the antimicrobial treatment

Continue the antimicrobial treatment for a duration predetermined by the investigator (usual practice, at least 5 days of treatment in total).

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Adult patient (≥18 years old)
• Admitted to hospital for suspected CAP defined by the presence of at least 2 of the following diagnostic clinical criteria:

• Fever (temperature > 38°C) or hypothermia (< 36°C)
• Dyspnea
• Cough
• Production of purulent sputum
• Crackles
• Radiological evidence of a new infiltrate (chest X-ray or CT scan)
• Negative viral respiratory testing
• Treated for a minimum of 48 hours with antibiotics (excluding azithromycin due to its prolonged half-life)Presenting with an early clinical response within the last 24 hours (up to 7 days after the start of antibiotic treatment, if planned treatment duration > 7 days), defined by the presence of all the following criteria:apyrexia (T°C ≤ 37.8)heart rate < 100/minrespiratory rate < 24/min, according to the patient's usual mode of oxygenation,arterial oxygen saturation ≥ 92%, according to the patient's usual mode of oxygenation,Patient currently under antibiotic treatment for his suspected CAP (i.e. the last dose of ATB has been administered to the patient less than 24 hours ago)
• Patient presenting a clinical response within the last 24 hours defined by the presence of all the following criteria:

• apyrexia (T°C ≤ 37.8)
• heart rate < 100/min
• respiratory rate < 24/min, according to the patient's usual mode of oxygenation,
• arterial oxygen saturation ≥ 92%, according to the patient's usual mode of oxygenation,
• systolic blood pressure ≥ 90mmHg, The last occurring of these criteria must have appeared within the last 24 hours.
• The antibiotic treatment for suspected CAP has started at least 48 hours ago and at most 6 days ago
• No other site of infection besides respiratory
• Affiliated to Health insurance
• Has given informed consent
• Patient understanding oral and written French, or presence of a relative who can explain and help him complete the study documents

Exclusion Criteria

• Signs of severe CAP (abscess, massive pleural effusion, serious chronic respiratory insufficiency)
• Known immunosuppression (asplenia, neutropenia, agammaglobulinemia, transplant, myeloma, lymphoma, known HIV and CD4<200/mm3)
• Suspected or confirmed legionellosis
• Any other infection necessitating concomitant antibiotic treatment
• Confirmed or suspected aspiration pneumonia or healthcare-associated pneumonia
• Treatment of suspected CAP with azithromycin (due to its prolonged half-life)
• Concomitant steroid treatment (only for patients treated with fluoroquinolones antibiotics)
• Pre-existing aortic aneurysm or dissection, family history of aortic aneurysm or dissection, Marfan syndrome, Ehlers-Danlos syndrome, Takayasu arthritis, uncontrolled arterial hypertension, atherosclerosis (only for patients treated with fluoroquinolones antibiotics)
• Pregnant or breastfeeding woman
• Life expectancy < 1 month
• Patient under legal guardianship (French "tutelle" or "curatelle")
• Patient without fixed address
• Patient enrolled in another interventional clinical trial on CAP treatment

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Aurélien Dihn, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Infectious diseases department, Raymond-Poincaré Hospital - APHP

Jacques Ropers, PharmD

Role: STUDY_DIRECTOR

Clinical Research Unit Pitié Salpêtrière - Charles Foix, CHU La Pitié-Salpêtrière - APHP

Locations

Infectious diseases department, Raymond-Poincaré Hospital - APHP

Garches, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Aurélien Dinh, MD, PhD

Role: CONTACT

aurelien.dinh@aphp.fr

+ 33 (0)1 47 10 44 32

Jacques Ropers, PharmD

Role: CONTACT

jacques.ropers@aphp.fr

+ 33 01 42 16 03 48

References

Dinh A, Ropers J, Duran C, Davido B, Deconinck L, Matt M, Senard O, Lagrange A, Makhloufi S, Mellon G, de Lastours V, Bouchand F, Mathieu E, Kahn JE, Rouveix E, Grenet J, Dumoulin J, Chinet T, Pepin M, Delcey V, Diamantis S, Benhamou D, Vitrat V, Dombret MC, Renaud B, Perronne C, Claessens YE, Labarere J, Bedos JP, Aegerter P, Cremieux AC; Pneumonia Short Treatment (PTC) Study Group. Discontinuing beta-lactam treatment after 3 days for patients with community-acquired pneumonia in non-critical care wards (PTC): a double-blind, randomised, placebo-controlled, non-inferiority trial. Lancet. 2021 Mar 27;397(10280):1195-1203. doi: 10.1016/S0140-6736(21)00313-5.

Reference Type: BACKGROUND

PMID: 33773631 (View on PubMed)

Other Identifiers

2023-504208-27-00

Identifier Type: OTHER

Identifier Source: secondary_id

APHP220814

Identifier Type: -

Identifier Source: org_study_id