- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06447220
Washed Microbiota Transplantation for Malnutrition
July 6, 2025 updated by: Faming Zhang, The Second Hospital of Nanjing Medical University
Malnutrition is a pathological condition in which dietary intake fails to meet the body's energetic or nutritional needs.
It may be caused by macronutrient or micronutrient deficiencies, high energy expenditure, impaired nutrient absorption or assimilation.
Malnutrition can affect all stages of life.
In adults, malnutrition is strongly associated with poor clinical outcomes such as increased morbidity, increased mortality and prolonged hospitalization.
In children, malnutrition can lead to growth retardation, cognitive impairment and immune dysfunction.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The gut microbiota of malnourished patients is different from that of healthy people.
The diversity of the gut microbiota of patients with severe malnutrition reduced and the abundance of Proteobacteria significantly increased, as well as pathogenic genera such as Klebsiella, Escherichia coli, Shigella, and Streptococcus.
This suggests that gut microbiota plays an important role in the occurrence and development of malnutrition.
Dietary intervention targeting gut microbiota can quickly improve children's malnutrition, promote weight gain and increase protein levels that promote bone growth and nerve development.
Exclusive enteral nutrition combined with immediate washed microbiota transplantation(WMT) can rapidly improve the nutritional status of patients with Crohn's disease compared with those with delayed WMT.
Gut microbiota has been confirmed to be closely related to malnutrition.
Improving the disordered gut microbiota in malnourished patients may become a potential treatment.
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Faming Zhang, PhD
- Phone Number: 086-025-58509883
- Email: fzhang@njmu.edu.cn
Study Contact Backup
- Name: Bota Cui, PhD
- Phone Number: 086-025-58509884
- Email: cuibota@njmu.edu.cn
Study Locations
-
-
Jiangsu
-
Nanjing, Jiangsu, China
- Recruiting
- Department of Microbiota Medicine & Medical Centre for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical University
-
Contact:
- Faming Zhang, PhD
- Phone Number: 086-025-58509883
- Email: fzhang@njmu.edu.cn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with malnutrition receiving WMT will be enrolled.
Description
Inclusion Criteria:
- Age ≥18 years old;
- Meet any of the following two conditions: ①weight loss (>5% weight loss in the past 6 months or >10% weight loss in more than 6 months); ②low BMI (<70 years old and BMI<18.5kg/m2 or ≥70 years old and BMI<22kg/m2);
- Underwent washed microbiota transplantation.
Exclusion Criteria:
- Expected survival time <3 months;
- Women who are pregnant or breastfeeding;
- Other patients deemed not suitable for enrollment by the investigator.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
The malnourished undergoing washed microbiota transplantation
patients undergoing washed microbiota transplantation who were diagnosed as malnutrition according to weight loss or low BMI
|
The prepared microbiota suspension was infused into the patients' gut.
Other Names:
|
|
The malnourished not undergoing washed microbiota transplantation
The malnourished patients did not undergo washed microbiota transplantation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change of the third lumbar vertebrae skeletal muscle mass and height
Time Frame: baseline, 12 weeks post transplantation
|
The third lumbar vertebrae skeletal muscle mass represents the sum of the cross-sectional areas of the skeletal muscles at the L3 level, including the psoas major, the erector spinae, the quadratus lumborum, the musculus transversus abdominis, the obliquus externus abdominis and the obliquus internus abdominis.
Skeletal muscle mass and height will be combined to report the third lumbar vertebrae skeletal muscle mass index(L3 SMI) in cm^2/m^2.
|
baseline, 12 weeks post transplantation
|
|
change of weight and height
Time Frame: baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
Weight and height will be combined to report BMI in kg/m^2.
|
baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change of the 5-level EuroQoL Group's 5-dimension (EQ-5D-5L)
Time Frame: baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
EQ-5D-5L is a 5-dimension questionnaire measuring health state and each dimension represents the level from 1 to 5, with higher level indicating worse health state.
|
baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
|
change of the Pittsburgh Sleep Quality Index (PSQI)
Time Frame: baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
PSQI is a self-rated questionnaire which assesses sleep quality over a 1-month time interval.
Nineteen items generate seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction.
The sum of scores for seven components yields one global score, with higher score indicating worse sleep quality.
|
baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
|
change of the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue)
Time Frame: baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
FACIT-Fatigue is a 13-item test measuring fatigue and each item receives a value from 0 to 4, with higher value indicating worse fatigue state.
|
baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
|
change of the Gastrointestinal Symptom Rating Scale(GSRS)
Time Frame: baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
GSRS is a 13-item test to make a comprehensive assessment of common gastrointestinal symptom and each item receives a value from 0 to 3, with higher value indicating worse gastrointestinal condition.
|
baseline, 4 weeks, 8 weeks, 12 weeks post transplantation
|
|
change of insulin-like growth factor I(IGF-I)
Time Frame: baseline, 12 weeks post transplantation
|
Blood is tested for Insulin-like growth factor I.
|
baseline, 12 weeks post transplantation
|
|
the difference of the gut microbiota composition before and after washed microbiota transplantation
Time Frame: baseline, 12 weeks post transplantation
|
The composition of the gut microbiota is evaluated by sequencing faecal metagenome.
We evaluate the differences in the structure of the flora and its metabolism.
|
baseline, 12 weeks post transplantation
|
|
the incidence of treatment-related adverse events (AE) assessed by CTCAE, Version 5.0
Time Frame: 12 weeks post transplantation
|
The severity of AE was graded as mild (grade 1), moderate (grade 2), severe/disabling (grade 3), life threatening (grade 4), and death (grade 5).
All AE were divided in definitely, probably and possibly related to treatment.
The treatment-related AE we focused on included microbiota-related AEs (e.g., infection, diarrhea, abdominal pain, etc.) and route of delivery related AEs (e.g., nausea, vomiting, etc.).
|
12 weeks post transplantation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Faming Zhang, PhD, The Second Hospital of Nanjing Medical University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Chen RY, Mostafa I, Hibberd MC, Das S, Mahfuz M, Naila NN, Islam MM, Huq S, Alam MA, Zaman MU, Raman AS, Webber D, Zhou C, Sundaresan V, Ahsan K, Meier MF, Barratt MJ, Ahmed T, Gordon JI. A Microbiota-Directed Food Intervention for Undernourished Children. N Engl J Med. 2021 Apr 22;384(16):1517-1528. doi: 10.1056/NEJMoa2023294. Epub 2021 Apr 7.
- Xiang L, Yu Y, Ding X, Zhang H, Wen Q, Cui B, Zhang F. Exclusive Enteral Nutrition Plus Immediate vs. Delayed Washed Microbiota Transplantation in Crohn's Disease With Malnutrition: A Randomized Pilot Study. Front Med (Lausanne). 2021 Oct 22;8:666062. doi: 10.3389/fmed.2021.666062. eCollection 2021.
- Miller J, Wells L, Nwulu U, Currow D, Johnson MJ, Skipworth RJE. Validated screening tools for the assessment of cachexia, sarcopenia, and malnutrition: a systematic review. Am J Clin Nutr. 2018 Dec 1;108(6):1196-1208. doi: 10.1093/ajcn/nqy244.
- Dent E, Wright ORL, Woo J, Hoogendijk EO. Malnutrition in older adults. Lancet. 2023 Mar 18;401(10380):951-966. doi: 10.1016/S0140-6736(22)02612-5. Epub 2023 Jan 27.
- Fontaine F, Turjeman S, Callens K, Koren O. The intersection of undernutrition, microbiome, and child development in the first years of life. Nat Commun. 2023 Jun 15;14(1):3554. doi: 10.1038/s41467-023-39285-9.
- Coley EJL, Hsiao EY. Malnutrition and the microbiome as modifiers of early neurodevelopment. Trends Neurosci. 2021 Sep;44(9):753-764. doi: 10.1016/j.tins.2021.06.004. Epub 2021 Jul 21.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 17, 2023
Primary Completion (Estimated)
December 1, 2030
Study Completion (Estimated)
April 1, 2031
Study Registration Dates
First Submitted
May 19, 2024
First Submitted That Met QC Criteria
June 5, 2024
First Posted (Actual)
June 7, 2024
Study Record Updates
Last Update Posted (Actual)
July 10, 2025
Last Update Submitted That Met QC Criteria
July 6, 2025
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WMT-MN-2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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