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Enterobacteriaceae InfectionsPhase 3FECESNCT05035342

Fecal Transplantation to Eradicate Colonizing Emergent Superbugs

A Phase 3 study testing Fecal Microbiota Transplantation (FMT) capsules in people with Enterobacteriaceae Infections and Fecal Microbiota Transplantation, run by Assistance Publique - Hôpitaux de Paris at 11 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Carriage of multi-drug and extensive-drug resistant Gram negative bacteria (MDR-GNB) is associated with an increased risk of infections by these bacteria for the carriers and a high risk of dissemination both in the healthcare setting and the community; the main MDR-GNB reservoir is the fecal microbiota. Read more about this study

Who is it for?
Ages 18 to 105 years
What is being tested?
Fecal Microbiota Transplantation (FMT) capsules
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
214 participants
Where
11 sitesFrance
Study dates
11 Jan 2024to Apr 2028
Phase
Phase 3
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 to 105 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • ≥ 18 years and < 105 years
  • Patient with at least one positive rectal swab for enterobacteria:
  • extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) or carbapenem-resistant Enterobacteriaceae (CRE), or who have had an ESBL-E or CRE infection within the year For ESBL-E carriers: an ESBL-E infection within the year is mandatory
  • Patient able to take 50 capsules orally in a day and without swallowing disorders
  • Healthy subjects ≥ 18 years and < 50 years
  • Body mass index < 30 kg/m^2
  • Regular bowel movement defined as at least 1 stool every 2 daysand maximum than 3 stools per day

Who cannot join

  • Current antibiotic treatment with te exception of long term antibiotic prophylaxis (duration of at least 3 months/year)
  • Patients hospitalized in the intensive care unit
  • Pregnancy or breastfeeding during the study
  • Women of childbearing potential who are unwilling or unable to use an acceptable method of birth control [such as oral contraceptives, other hormonal contraceptives (vaginal products, skin patches, or implanted or injectable products), or mechanical products such as an intrauterine device or barrier methods (condoms)] to avoid pregnancy for the entire study
  • Patient under legal protection
  • Participation in another interventional study
Show all 19Show fewer
  • Non-affiliation to a social security scheme
  • Patient under AME
  • Refusal to participate to the study
  • Any history of or current proctologic disease or any acute condition, which in the investigator's judgment could harm the volunteer and/or compromise or limit the evaluation of the protocol or data analysis (for details, please see protocol)
  • Subject under legal protection
  • Participation in any other interventional study
  • No-affiliation to a social security scheme
  • Subject under AME
  • Refusal to participate to the study
  • Randomization criteria:
  • Patient colonized with a carbapenem-resistant Enterobacteriaceae (CRE) and/or colonized with an extended spectrum β-lactamase producing Enterobacteriaceae (ESBL-E) at inclusion on stool culture
  • Patient with an ESBL-E infection in the previous 12 months (only for participants no colonized with CRE).
  • Compatible transplant (FMT) based on patient's serological profile (CMV/EBV) available

Trial locations and contacts

11 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Victoire De Lastours, MD, PhD contact

+33 1 40 87 52 27

victoire.de-lastours@aphp.fr

Harry Sokol, MD, PhD contact

+33 1 49 28 24 73

harry.sokol@aphp.fr

11 sites in 1 country

France11 sites, 11 recruiting
  • Beaujon Hospital

    Clichy

    Victoire DE LASTOURS

    Agnès LEFORT

    Not yet recruiting
  • Henri Mondor Hospital

    Créteil

    Raphael LEPEULE

    Not yet recruiting
  • Raymond Poincaré Hospital

    Garche

    Benjamin DAVIDO

    Not yet recruiting
  • Bicêtre Hospital

    Le Kremlin-Bicêtre

    Lelia ESCAUT

    Not yet recruiting
  • Bichat Hospital

    Paris

    Solen KERNEIS

    Not yet recruiting
  • Bichat Hospital

    Paris

    Xavier DUVAL

    Recruiting
  • La Pitié Salpêtrière Hospital

    Paris

    Alexandre BLEIBTREU

    Not yet recruiting
  • Lariboisière Hospital

    Paris

    Anne Lise MUNIER

    Not yet recruiting
  • Saint Antoine Hospital

    Paris

    Laure SURGERS

    Not yet recruiting
  • Saint Louis Hospital

    Paris

    Matthieu LAFAURIE

    Not yet recruiting
  • Tenon Hospital

    Paris

    Ruxandra CALIN

    Not yet recruiting

Other trials in France

About this study

Carriage of multi-drug and extensive-drug resistant Gram negative bacteria (MDR-GNB) is associated with an increased risk of infections by these bacteria for the carriers and a high risk of dissemination both in the healthcare setting and the community; the main MDR-GNB reservoir is the fecal microbiota. To prevent both infections and dissemination, effective measures to decolonize subjects carrying MDR-GNB are urgently needed. Animal models, case reports and cohort studies suggest fecal microbiota transplantation (FMT) may be efficient for MDR-GNB decolonization.

Read the detailed description

The issue of antibiotic resistance is considered as one of the major Public Health threats of the 21th century by the World Health Organisation (WHO). Given the rapid increase in the dissemination of multi-drug resistant organisms globally, the real implications of spreading drug resistance will be felt the world over, with developing countries and large emerging nations bearing the brunt of this problem. Routine surgeries and minor infections will become life-threatening once again and the hard won victories against infectious diseases of the last fifty years will be jeopardised. Hospital stays and expenses will increase significantly. Drug resistant infections are already on the rise with numbers suggesting that up to 50,000 lives are lost each year to antibiotic-resistant infections in Europe and the US alone. Globally, at least 700,000 die each year of drug resistance in bacterial infections. Estimates have found that antibiotic resistance may kill more than cancer in 2050, with figures reaching 10 million deaths a year globally, if nothing is done.

In this context, one of the most worrying problems is the dramatic increase in infections caused by multi-drug resistant Gram Negative bacteria (MDR-GNB), including extended spectrum β-lactamase and/or carbapenem-resistant Enterobacteriaceae (ESBL-E and CRE) with few effective therapeutic options remaining in the armamentarium of clinicians. There is a striking lack of new antimicrobial agents especially against MDR-GNB while dissemination of these MDR-GNB is accelerating. The rising epidemic of CRE is especially worrying. Southern European countries such as Italy and Greece are already at epidemic levels of CRE infections, which are associated with much higher death rates and are more expensive to treat because of the lack of effective non-toxic antibiotics.

Even if new agents were discovered, the lead in time is considerable as there are no truly new agents expected on the market in the short or medium term. Alternative effective measures to contain resistance and limit the spread of MDR-GNB are therefore urgently needed. The gut microbiota is the main reservoir of MDR-GNB. Patients carrying MDR-GNB are at higher risk of clinical infections with their own bacteria and of dissemination in the community and in the hospital settings. In the last 10 years, the number of MDR-GNB carriers has increased strikingly (for instance, one report found a 10-fold increase in France from 2006-2011 from 0.6% to 6% of subjects in the community; another found a 12% ESBL-E colonization rate in Parisian hospitals upon admission in 2015) and continues to rise. Finding efficient decolonization strategies is urgent to attempt to limit the risk of infection at the individual level and the spread of MDR-GNB at the population level.

Fecal microbiota transplantation (FMT), which has been shown to be highly effective for the treatment of recurrent Clostridium difficile infections (CDI), has also been suggested as a decolonization strategy for patients carrying MDR-GNB: animal models and several clinical case reports suggest that this strategy may be interesting to decolonize MDR-GNB carriers. To date, the question of whether FMT may be efficient to decolonize MDR-GNB carriers in human is not resolved. Because decolonization may also be spontaneous, performing a randomized controlled trial is essential to answer this question.

The hypothesis for this study is that FMT may be efficient to decolonize patients carrying MDR-GNB in their gut microbiota. To determine whether this hypothesis is true, we shall conduct a phase III randomized controlled trial comparing capsule-delivered FMT with a placebo to decolonize subjects carrying either CRE or ESBL-E.

Elimination of carriage should benefit directly the individual patient by preventing infections with these resistant organisms and limiting isolation precautions, which impacts their quality of care, the possibilities of transfer to other healthcare settings (such as rehabilitation centres) and their psychological health. Additionally, the elimination of MDR-GNB carriage should benefit the community by decreasing the risk of inter-individual transmission in particular in the healthcare setting. For this intervention, we will use frozen capsules rather than nasogastric infusion or colonoscopy, as they limit adverse events, facilitate donor screening, allow for outpatient treatment, and are adapted to treat large populations. Thanks to the above-mentioned reasons, capsules are becoming the standard-of-care for FMT. In the context of the major threat that antibiotic resistance in Gram negatives carries, both on an individual and a collective point-of-view; this is a highly important question.

Being tested
Fecal Microbiota Transplantation (FMT) capsules, Placebo capsules
Medical subject headings
Enterobacteriaceae Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fecal Microbiota Transplantation (FMT) capsulesBiological

    Donated fecal matter will be sequentially diluted in 80% glycerol used as bacterial cryoprotectant, blenderized, sieved and centrifuged (4°C, 4000 tr/min, 20 min). The pellet is resuspended and manually pipetted into size 0 capsules (650 μL), which are closed and then secondarily sealed in size 00 capsules (hypromellose capsules, DR caps from Capsugel®, MA). Each capsule contains 1g ± 0,1g of fecal suspension corresponding to 0.5 to 0.8g of native stool. Capsules will be stored frozen at -80°C for up to 24 months pending use. The stability of biodiversity and viability of the frozen microbiota was regularly verified to ensure the efficacy of the transplantation (personal data).

  • Placebo capsulesBiological

    The "placebo" FMT capsules will be performed with the final dilution solution, ie the 80% glycerol solution used as a cryoprotectant. This solution will be double encapsulated like the FMT capsules.

Study groups in NCT05035342
Study groupRoleWhat they receive
Fecal microbiota Transplant (FMT)ExperimentalFecal microbiota Transplant (FMT) prepared from the stools of healthy donors diluted in 80% glycerol used as bacterial cryoprotectant, blenderized, sieved and centrifuged (4°C, 4000 tr/min, 20 min) and manufactured in capsules (n=50 capsules corresponding to approximately 50 grams of stool; 50 in one day).
Receives: Biological: Fecal Microbiota Transplantation (FMT) capsules
Placebo of FMTPlacebo comparatorFMT vehicle (solution of saline (NaCl 0.9%)) with 80% glycerol (storage in the same conditions as preparation for FMT experimental group) administered at the same volume and same time point as the experimental group.
Receives: Biological: Placebo capsules

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Determine whether FMT with frozen capsules is effective for decolonization of MDR-GNB.

    Proportion of subjects not carrying MDR-GNB (neither ESBL-E nor CRE) at day 30 (±10 days) after randomization as determined by culture methods

    Measured: 30 days post-randomization

Secondary outcomes (10)
  1. Prevention of infections

    Occurrence of a clinical infection with ESBL-E or CRE, between randomization and day 90

    Measured: 90 days post-randomization

  2. Prevention of infections

    Number of days of use of systemic antibiotics between randomization and day 90

    Measured: 90 days post-randomization

  3. Prevention of infections

    Number of days of isolation precautions during the hospital stay

    Measured: up to 2 years post-randomization

  4. Prevention of infections

    Length of stay in hospital

    Measured: up to 2 years post-randomization

  5. Safety and tolerability of FMT

    Incidence of Treatment-Emergent Adverse Events

    Measured: 2 years post-randomization

  6. Microbiology

    Proportion of subjects not carrying MDR-GNB (neither ESBL-E nor CRE) at day 90 after randomization

    Measured: 90 days post-randomization

  7. Microbiology

    Relative abundance of resistant strains over the total Enterobacteriaceae (expressed as a ratio)

    Measured: Baseline (inclusion), 30 and 90 days post-randomization

  8. Microbiology

    Concentration (expressed in colony-forming units per gram of feces) of resistant strains

    Measured: Baseline (inclusion), 30 and 90 days post-randomization

  9. Microbiology

    Characteristics of ESBL-E/CPE strains (species identification, resistance mechanisms)

    Measured: Baseline (inclusion), 30 and 90 days post-randomization

  10. Microbiology

    16S microbiome analysis, analysis in terms of diversity and operational taxonomic unit (OTU) presence (relative to baseline)

    Measured: Baseline (inclusion), 30 and 90 days post-randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Sep 2021
  2. Study start11 Jan 2024
  3. Primary completionMay 2026 (estimated)
  4. Study completionApr 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
Double-blinded placebo-controlled randomized multicentric controlled trial with a 1:1 randomization.
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
214 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05035342
Sponsor's protocol ID
APHP180587
Other IDs
2019-004402-10, 2019
Acronym
FECES
Status last verified
May 2025
First submitted
31 Jul 2021
Last updated
25 May 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Fecal Microbiota Transplantation (FMT) capsules in people with Enterobacteriaceae Infections and Fecal Microbiota Transplantation, run by Assistance Publique - Hôpitaux de Paris at 11 sites in France.

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 7 inclusion and 19 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: looking for participants now, as of the sponsor's last update on 25 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 11 sites in France. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

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 Victoire De Lastours, MD, PhD (+33 1 40 87 52 27, victoire.de-lastours@aphp.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Determine whether FMT with frozen capsules is effective for decolonization of MDR-GNB. (time frame: 30 days post-randomization). 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 25 May 2025.

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