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Intestinal Microbiome and Chemotherapy

Chemotherapy-driven Dysbiosis in the Intestinal Microbiome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02875249
Acronym
EMAAD
Enrollment
40
Registered
2016-08-23
Start date
2010-11-01
Completion date
2014-01-01
Last updated
2026-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diarrhea

Keywords

post-antibiotic diarrhea, intestinal microbiome

Brief summary

Chemotherapy is commonly used as myeloablative conditioning treatment to prepare patients for haematopoietic stem cell transplantation (HSCT). Chemotherapy leads to several side effects, with gastrointestinal (GI) mucositis being one of the most frequent. Current models of GI mucositis pathophysiology are generally silent on the role of the intestinal microbiome. The aim of the study is to identify functional mechanisms by which the intestinal microbiome may play a key role in the pathophysiology of GI mucositis, the investigators applied high throughput DNA-sequencing analysis to identify microbes and microbial functions that are modulated following chemotherapy.

Interventions

OTHERpatients stool collection

patients stool collection

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants with non-Hodgkin's lymphoma * Participants receiving the same myeloablative conditioning regimen for five consecutive days, including high-dose Carmustine (Bis-chloroethylnitrosourea), Etoposide, Aracytine and Melphalan.

Exclusion criteria

* Patients with a history of Inflammatory Bowel Diseases (IBD), exposed to probiotics, prebiotics or broad-spectrum antibiotics, or administered nasal-tube feeding or parenteral nutrition in the month prior to initiation of the study.

Design outcomes

Primary

MeasureTime frame
analyze of the fecal samples using 16S ribosomal ribonucleic acid (rRNA) gene sequencingbaseline

Countries

France

Contacts

PRINCIPAL_INVESTIGATOREmmanuel Montassier, PH

Nantes Univetsity Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026