Gut bacteria may control immune cell fuel – new study investigates
NCT ID NCT07300553
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looks at how gut bacteria change the energy use of immune cells in people with inflammatory bowel disease (IBD) and healthy adults. Researchers will give healthy volunteers a short course of antibiotics to alter their gut bacteria, then measure immune cell metabolism using a special blood test. IBD patients will be tested once without antibiotics. Participants will also consume a labeled fiber to track how gut bacteria break it down. The goal is to understand the link between gut microbes and immune cell function, which could lead to better treatments for IBD.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Vancomycin, Amphotericin B, Gentamicin (antibiotics and antifungal)
- What this could lead to
- If successful, this could reveal how gut bacteria influence immune cell energy, pointing toward new ways to manage inflammatory bowel disease.
- What could go wrong
- This is a small, early-phase study with only 45 participants. It aims to understand mechanisms, not test a treatment, so direct patient benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 45 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Healthy volunteer 1. Age ≥ 18 years and \< 50 years 2. 17 kg/m² \< body mass index \< 25 kg/m² (microbiota modified based on BMI, (Le Chatelier et al., 2013) 3. For women, female of child-bearing age with an active contraception (hormonal, intrauterine device, bilateral tubal occlusion, sexual abstinence\*) and this during at least the period of treatment (up to v2) \*Sexual abstinence is defined as refraining from heterosexual intercourse from providing consent until V3. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the study and the preferred and usual lifestyle of the participant * A woman is considered of childbearing potential, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH), level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient 4. Regular bowel movement defined as at least 1 stool every other day and maximum 3 stools per day 5. Patient with health insurance (AME except) 6. Informed Written consent Patient with IBD <!-- --> 1. Age ≥ 18 years and \< 50 years 2. Crohn's Disease (Excepting disease involving only the upper GI tract) or ulcerative colitis (excepting disease involving only the rectum), according to the Lennard-Jones criteria for at least 6 months (15 patients with Crohn's disease and 15 with ulcerative colitis will be recruited) 3. Patient in steroid-free clinical remission for at least 6 months (for Crohn's disease: CDAI \<150 the week before inclusion, for ulcerative colitis: Partial Mayo Clinic score of 0 or 1). 4. 17 kg/m² \< body mass index \< 25 kg/m² 5. Female of child-bearing age with an active contraception. Efficient contraception include oral contraception, intrauterine devices hormonal device, intrauterine hormone-releasing system, sterilization method and other forms of contraception with failure rate \<1%) \*\* A woman is considered of childbearing potential, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient 6. Regular bowel movement defined as at least 1 stool every other day and maximum 3 stools per day 7. Patient with health insurance (AME except) 8. Informed Written consent Non inclusion Criteria: Healthy volunteers 1. Significant chronic disease and particularly chronic gastrointestinal diseases, type 1 and type 2 diabetes, renal alteration 2. Curative long-term treatment 3. Pregnant or breastfeeding women\*\* \*\* A woman is considered of childbearing potential, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a post-menopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient. 4. blood donation in the 3 months before the study 5. Taking antibiotic or antifungal (oral) in the previous 3 months before planned day 0 (V1) 6. probiotics in the month preceding day 0 (V1), 7. consumption of a low-calorie diet or any other special diet (except vegetarian) in the month before day 0 8. abdominal surgery in the past (except for appendectomy) 9. allergy against the antibiotics and antifungal treatment used in this study or to their excipients 10. contra-indications to the administration of gentamicin (refer to SmPC) 11. Participation in any other interventional study 12. Patients under legal protection Patients with IBD <!-- --> 1. Pregnant or breastfeeding women 2. blood donation in the 3 months before the study 3. Taking antibiotic or antifungal (oral) in the previous 3 months before planned day 0 4. probiotics in the month preceding day 0 and during the study, 5. Ileal resection \> 50cm or colectomy 6. Diagnosis of Crohn's disease restricted to the upper gastrointestinal tract (oesophagus, stomac, duodenum, jejunum) 7. Diagnosis of ulcerative colitis restricted to the rectum. 8. Current stoma (Ileostomy or a colostomy) or stoma in the last 6 months or any other intra-abdominal surgery within 3 months prior to inclusion 9. Participation in any other interventional study 10. Patients under legal protection Exclusion Criteria: Healthy volunteers : * Clinically significant abnormal serum/ plasma levels of electrolytes, creatinine, liver enzymes, thyroid stimulating hormone or blood cell count at the biological check-up of the visit v0 (screening and inclusion) * Infectious episode requiring antimicrobial treatment since V0 * Severe diarrhea (increase of seven or more stools per day over baseline) Patients with IBD - Infectious episode requiring antimicrobial treatment since V0 \- IBD flare
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Gastroenterology Department Saint Antoine Hospital,
RECRUITINGParis, 75012, France
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Other studies related to the condition(s) this trial covers.
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- Two biologics go head to head in ulcerative colitis
- Can a liquid diet calm Crohn's in kids?
- New drug ATTO-1091 put to the test for safety in ulcerative colitis
- Antiparasitic drug tested as new weapon against ulcerative colitis