Overview
This is a observational study to explore the efficacy and safety of washed microbiota transplantation (WMT) combined with nutritional support for gastroptosis patients
Eligibility
Inclusion Criteria:
- Subjects must meet all of the following inclusion criteria to enter the study:
- Clinically diagnosed with gastroptosis;
- Meets the diagnostic criteria for malnutrition (fulfilling any one of the following two criteria):
- Weight loss (weight loss \>5% within the last 6 months or \>10% over more than 6 months);
- Low BMI (BMI \<18.5 kg/m² for individuals \<70 years old; BMI \<20 kg/m² for individuals ≥70 years old);
- Weight loss (weight loss \>5% within the last 6 months or \>10% over more than 6 months);
- Males aged ≥18 years and non-pregnant, non-lactating females aged ≥18 years;
- Willing to voluntarily sign a written informed consent form and agrees to follow medical advice for regular follow-up examinations and monitoring after the completion of treatment.
Exclusion Criteria:
- Subjects meeting any of the following exclusion criteria must be excluded from the study:
- Patients with severe depression, anxiety, or cognitive impairment that affects normal physician-patient communication and treatment planning;
- Patients with poor compliance who cannot accept treatment regimens such as nasogastric enteral nutrition;
- Anticipated survival time \<3 months;
- Clinically significant cardiovascular diseases, including heart failure (NYHA Class III-IV), uncontrolled coronary artery disease, cardiomyopathy, arrhythmia, history of myocardial infarction, hemodynamic instability at enrollment, unstable vital signs, or anticipated risk events during treatment;
- Poor pulmonary function deemed by investigators to impact study treatment (e.g., acute exacerbation of COPD or requirement for long-term oral/intravenous corticosteroids \[excluding inhaled corticosteroids\]);
- Active severe clinical infections (\> Grade 2 per NCI-CTCAE v5.0), including patients with intestinal fungal, viral, or tuberculosis infections;
- Inability to cooperate with intestinal tube placement or contraindications to intestinal tube placement;
- Use of medications affecting or modulating gut microbiota within the past 48 hours;
- Lack of legal capacity or restricted legal capacity;
- Hematologic disorders unsuitable for blood draw examinations;
- Other severe medical conditions deemed by investigators to preclude patient enrollment.


