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NCT Number: NCT06478823

Healthy Stool Volunteer Donors for Fecal Microbiota Transplantation Trials

Currently, ANSM recommendations govern FMT (Fecal Microbiota Transplantation) in clinical trials. The collection and validation of these stool donations as part of the trials is complex and not very efficient. It therefore seems essential to identify the limiting factors and the characteristics of Healthy Volunteer Donors to optimize the number of valid stool donations.

Recruiting

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Key information

Age range

18 year–49 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

If the ANSM recommendations govern FMT (Fecal Microbiota Transplantation) in clinical trials, the selection, inclusion of Healthy Volunteer Donors (HVD), then the collection and validation of these stool donations is complex and not very effective. It therefore seems essential to identify the limiting factors and the characteristics of HVD to optimize the number of valid stool donations.

Healthy voluntary donors of stools for the preparation of TMF (Healthy Volunteer Donors, -TMF) for trials to evaluate its effectiveness in various pathologies will be selected, included and followed in a common protocol (ANSM agreement obtained) in order to facilitate this entire process and pool resources. This will allow us to describe the clinical characteristics and lifestyle habits of Healthy Volunteer Donors associated with the validity of stool donations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years and < 50 years
  • 17 kg/m² < body mass index < 30 kg/m²
  • Regular bowel movement defined as at least 1 stool every other day and maximum 2 stools per day
  • Subject with health insurance (AME excepted)
  • Informed written consent

Exclusion criteria

Definitive non-inclusion criteria:

  • Infectious risk :
  • Known HIV, HBV, HCV, HTLV infection
  • Residence of more than 2 years in the intertropics zone within the previous 5 years
  • Hospitalization abroad for more than 24 hours in the last 12 months (including a member of the healthy volunteers donor's entourage)
  • Risk factors for Creutzfeldt-Jakob disease (history: treatment with extractive growth hormone, a family case of transmissible spongiform subacute encephalopathy, surgery with opening of the dura or neurosurgery or invasive brain exploration before 1 January 1995, stay in United Kingdom for a duration greater than 1 year cumulatively between 1980 and 1996 or the presence of neurological or neuropsychiatric scalable recent clinical signs)
  • Previous history of typhoid fever, tuberculosis and malaria
  • Past or current injection drug user or regular use of other drug
  • Gastrointestinal disease:
  • Personal or 1st degree family history of: inflammatory bowel disease or celiac disease
  • Personal history of irritable bowel syndrome
  • Previous history of gastrointestinal neoplasia or polyps
  • Family history of 1st degree gastrointestinal neoplasia or polyps before age 60
  • 1st degree family history of one of the following autoimmune or inflammatory disease : inflammatory arthritis, psoriasis, multiple sclerosis, type I diabetes, spondylitis, lupus and Basedow disease
  • If family history unknown in the first degree, the donor is not eligible
  • Previous history of :
  • Subject prone to hemorrhoids (at least 1 event within the previous 1 year)
  • Subject with an active chronic illness (except active chronic mild allergic disease o (example: allergic rhinitis, chronic eczema…)) o Diagnosis of Gilbert's syndrome done by screening is not a chronic disease. The healthy volunteer donor will therefore remain eligible.
  • Serious allergy requiring hospitalization within the previous 12 months
  • Curative long-term treatment
  • Severe allergy requiring hospitalization in the last 12 months
  • Allogeneic human or animal tissue or organ transplant
  • Factors that may affect the composition of the intestinal microbiota:
  • Special Diet (example: gluten-free...)
  • Lactose-free, vegetarian and vegan diets are permitted.
  • Pregnancy or breastfeeding
  • Taking immunosuppressants (eg calcineurin inhibitors, corticosteroids, biological agents, etc.)
  • Antineoplastic chemotherapy
  • Subject under legal protection
  • Participation in any other interventional study except studies for stool donation

Temporary non-inclusion criteria

  • Infectious risk :
  • Unprotected sexual intercourse with a new partner in the previous 4 months and/or sexual intercourse with several different persons within the previous 4 months
  • sexual partner who has had more than 1 partner within the previous 4 months and/or
  • sexual transmitted infection within the previous 4 months (healthy volunteer donor himself or sexual partner)
  • Sexual relationship in exchange for money or drugs in the last 12 months. (healthy volunteer donor himself or sexual partner)
  • Sexual relationship with a partner with positive serology for HIV, viral hepatitis B or C, in the last 6 months.
  • Sexual relationship with a partner who has used intravenous drugs, doping substances
  • Hospitalization abroad for more than 24 hours in the last 12 months (healthy volunteer or entourage)
  • Travelling within the previous 6 months except : Germany, Austria, Belgium, Spain, Finland, Ireland, Italia, Luxembourg, Netherland, Portugal, Greece, Slovenia, Cyprus, Malta, Slovakia, Estonia , Bulgaria, Croatia , Hungary, Latvia , Lithuania, Poland , Romania, Czech Republic, the United Kingdom, Denmark, Norway, Sweden, Switzerland, USA, Iceland, Australia New Zealand, Japan, South Korea, Singapore, Israel or Canada.
  • Blood transfusion, piercing (including earrings) or tattoo within the previous 4 months
  • Surgery (all types) or hospitalization within the previous 4 months
  • Person living under the same roof or sexual partner with an infectious or contagious disease (i.e who have been hospitalized) within the previous 4 months
  • Blood exposure accident (for wound, pricking or projection ...) within the previous 4 months
  • Dental care within the previous 7 days
  • Gastroenteritis within the previous 3 months (defined by acute onset of diarrhea (> 3 soft or liquid stools per day) and duration < one week)
  • Episode of infection or skin infection/lesion within the previous 15 days 2-Risk linked to Covid-19
  • Confirmed infection in the previous 28 days (after symptoms have ceased)
  • Clinical signs of suspected infection (chill, cough, fever, dyspnea, myalgia, asthenia, malaise, pharyngeal pain, anosmia , ageusia, rhinorrhea, chest pain, headache, diarrhea) in the previous 28 days (after the end of symptoms)
  • Having been in risky contact (according to the definition of Santé Publique France with a person whose infection is confirmed or suspected: "14 days after the last risky contact: if the recommended screening tests in the event of risky contact between D15-D28 are negative "In the 28 days preceding inclusion in the absence of a screening test. Healthcare professionals using recommended protective measures with COVID patients are not considered high-risk contacts 3- Monkeypox risk
  • Confirmed or suspected infection within the previous 42 days ( after beginning of symptoms)
  • Risky contact with a person with confirmed or suspected infection within the previous 21 days (from the date of last contact)

4- vaccination with a live attenuated vaccine during the last month 5- Chronic diarrhoea in the previous 3 months or chronic constipation (fewer than 3 bowel movements per week for more than 6 months) 6- Excessive alcohol consumption in the last 4 months. (French Public Health definition: 10 standard drinks per week and a maximum of 2 drinks per day)

7 - Factors that may affect the composition of the intestinal microbiota:

  • Taking antibiotic or antifungal (oral) in the previous 3 months before donation
  • Taking non-steroidal anti-inflammatory drugs (oral) in the previous month before donation
  • Taking corticosteroids (oral) in the previous 4 weeks before donation. Corticosteroids allowed if taken more than 4 weeks before donation. and not for an autoimmune or inflammatory disease.

Temporary or permanent exclusion criteria:

  • At each visit of the donation period, the temporary or definitive exclusion criteria (identical to the temporary or definitive non-inclusion criteria) will be rechecked

Treatment and study plan

Stools donation

Other

Healthy volunteer donors included in the selection process to donate stool for the preparation of a TMF as part of research projects.

Donors will be followed from their selection until 6 months after their last valid stool donation.

Primary outcomes

  1. Proportion of HVD included who made at least 1 valid stool donation in the 12 months following their inclusion

    Time frame: 12 months

    A valid stool donation is a donation that complies with all the clinical and biological recommendations of the ANSM (Defining the rules of good practice relating to the collection, control, storage, traceability and transport of human stool samples as provided for in Article L. 513-11-2 of the Public Health Code. Decision of 7 April 2025.")

    Define among the Healthy Volunteer Donors-TMFs (HVD ) included, the number of (HVD ) having made at least 1 valid stool donation.

Secondary outcomes

  1. Proportion of "good donors": included donors having made at least 5 valid stool donations in the 12 months following their inclusion.

    Time frame: 12 months

    A valid stool donation is a donation that complies with all the clinical and biological recommendations of the ANSM

    Define among HVD included, "good donors" having made at least 5 valid stool donations

  2. Description of the clinical characteristics of HVD performing stool donation

    Time frame: 12 months

    Description of clinical characteristics (average age, average BMI) of donors who made at least 1 valid stool donation within 12 months following their inclusion and comparison with those of donors who did not not having made valid donations.

  3. Description of the lifestyle habits of HVD performing stool donation

    Time frame: 12 months

    Description of the lifestyle habits (lifestyle : profession, eating habits) of donors who made at least 1 valid stool donation within 12 months following their inclusion and comparison with those of donors who did not not having made valid donations.

  4. Reasons for non-eligibility during the inclusion visit or during the phone screening

    Time frame: 5 years

    Description of the reasons for non-eligibility during the inclusion visit or during the phone screening (non-inclusion criteria, availability, tolerance/acceptance of blood and nasopharyngeal samples, geographical distance, compensation amount, etc.) in order to evaluate the factors limiting the eligibility of HVD

  5. Factors limiting the number of donations made by HVD per donation period of 28 days maximum

    Time frame: 12 months

    Reasons for not carrying out or no preparation stool donation: availability HVD , ability to make a donation in hospital, tolerance/acceptance of blood and nasopharyngeal samples, possibility of stool preparation at the pharmacy, biological abnormalities, criteria for transitional or permanent exclusions

  6. Evaluate the membership of participation of HVD

    Time frame: 5 years

    Number of periods of donations made, regularity of donations, motivation for participation in the study collected by the investigator

  7. Evaluate the duration of participation of HVD

    Time frame: 5 years

    Duration of participation in the study collected by the investigator

  8. Reasons for premature termination or non-validation of stools

    Time frame: 5 years

    Reasons for premature termination or non-validation of stools: biological, viral, bacteriological, hematological abnormalities, HVD clinical anomaly, investigator decision HVD decision in order to assess the causes of premature termination of HVD and non-validation of stool donations

  9. Assess the characteristics of the microbiota of valid donations

    Time frame: 5 years

    Composition of the microbiota of HVD

Study contacts

Contact information is provided by the study sponsor or research team.

Harry SOKOL

CONTACT

[email protected]

00 33 1 49 28 31 62

Mélissa Montil, Praticien attaché

CONTACT

[email protected]

00 33 1 71 97 08 10

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • CRB-SAT BARM APHP.SU
  • CRSA UMRS 938

Registry information

Acronym: VIOLONSEL

Important dates

Study start
2024
Primary completion
2030
Study completion
2030
First posted
Jun 27, 2024
Registry last updated
Jul 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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